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Journal articles on the topic 'Propenamides'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Andreev, Mikhail V., Vladimir A. Potapov, Maxim V. Musalov, and Lyudmila I. Larina. "First Examples of Reactions of 3-Trimethylsilyl-2-Propynamides and Organic Diselenides: Synthesis of Novel Derivatives of Propynamides." Catalysts 13, no. 10 (2023): 1326. http://dx.doi.org/10.3390/catal13101326.

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First examples of the reactions of 3-trimethylsilyl-2-propynamides with organic diselenides yielding 3-alkylselanyl-2-propenamides and 3-organylselanyl-2-propynamides were realized. The latter compounds were obtained by the Cu-catalyzed reaction of organic diselenides with 4-propioloylmorpholine. The reaction of 3-trimethylsilyl-2-propynamides with dialkyl diselenides in the system NaBH4/H2O/K2CO3/THF proceeded in a regio- and stereoselective fashion, affording 3-alkylselanyl-2-propenamides in 90–94% yields. An unsymmetrical divinyl selenide with the cyclic amide groups and a product, containi

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2

V. Andreev, Mikhail, Vladimir A. Potapov, Maxim V. Musalov, and Svetlana V. Amosova. "(Z,Z)-Selanediylbis(2-propenamides): Novel Class of Organoselenium Compounds with High Glutathione Peroxidase-Like Activity. Regio- and Stereoselective Reaction of Sodium Selenide with 3-Trimethylsilyl-2-propynamides." Molecules 25, no. 24 (2020): 5940. http://dx.doi.org/10.3390/molecules25245940.

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The efficient regio- and stereoselective synthesis of (Z,Z)-3,3′-selanediylbis(2-propenamides) in 76–93% yields was developed based on the reaction of sodium selenide with 3-trimethylsilyl-2-propynamides. (Z,Z)-3,3′-Selanediylbis(2-propenamides) are a novel class of organoselenium compounds. To date, not a single representative of 3,3′-selanediylbis(2-propenamides) has been described in the literature. Studying glutathione peroxidase-like properties by a model reaction showed that the activity of the obtained products significantly varies depending on the organic moieties in the amide group. D

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3

Martinez, Roberto, Luis Velasco, Lino Reyes T., Rocio Pozas H., Javier A. Carballo P., and Patricia Melchor M. "Electron impact mass spectrometry of N-(2-methylpropyl)-3-(o-,m- andp-R-phenyl)-2-propenamidesl." Spectroscopy 12, no. 1 (1994): 9–20. http://dx.doi.org/10.1155/1994/637030.

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4

Štetinová, Jarmila, Rudolf Kada, Ján Leško, Lubomír Zalibera, Dušan Ilavský, and Alexander Bartovič. "Synthesis and Properties of Substituted 1-(2-Benzothiazolyl)-2-pyridones." Collection of Czechoslovak Chemical Communications 60, no. 6 (1995): 999–1008. http://dx.doi.org/10.1135/cccc19950999.

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The studied 1-(2-benzothiazolyl)-2-pyridones Va-Vf were prepared from N-(2-benzothiazolyl)cyanoacetamide (II) which on reaction with 4-substituted benzaldehydes afforded 3-aryl-N-(2-benzothiazolyl)-2-cyano-2-propenamides IVa-IVg. Compounds IVa-IVf were cyclized with malonodinitrile in the presence of piperidine to give the corresponding pyridones Va-Vf.

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5

Štetinová, Jarmila, Rudolf Kada, Ján Leško, Miloslava Dandárová, and Marcela Krublová. "Synthesis and Spectral Properties of 1-(6-Methoxy-2-benzothiazolyl)-2-pyridones." Collection of Czechoslovak Chemical Communications 61, no. 6 (1996): 921–29. http://dx.doi.org/10.1135/cccc19960921.

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Substituted 1-(6-methoxy-2-benzothiazolyl)-2-pyridones 5a-5f have been prepared from N-(6-methoxy-2-benzothiazolyl)cyanoacetamide (2) which on reactions with 4-substituted benzaldehydes gives 3-aryl-2-cyano-N-(6-methoxy-2-benzothiazolyl)-2-propenamides 4a-4g. Derivatives 4a-4f were cyclized with malonodinitrile in the presence of piperidine to give the corresponding 2-pyridones 5a-5f. The IR, UV, 1H NMR and mass spectra of the substances synthesized are discussed.

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6

BouzBouz, Samir. "ChemInform Abstract: Synthesis and Reactivity of New Chiral 1-[(Trialkylsilyl)methyl]propenamides." ChemInform 42, no. 52 (2011): no. http://dx.doi.org/10.1002/chin.201152189.

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7

Kharas, Gregory B., Benjamin L. Hill, Monica V. Garcia, et al. "Novel Copolymers of Styrene. 8. Ring-Trisubstituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 5 (2015): 331–35. http://dx.doi.org/10.1080/10601325.2015.1018802.

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8

Kharas, Gregory B., Najib J. Ayman, Rocelyn Calso, et al. "Novel Copolymers of Styrene. 11. Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 6 (2015): 412–16. http://dx.doi.org/10.1080/10601325.2015.1029365.

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9

BouzBouz, Samir. "Studies in the Synthesis and Reactivity of New Chiral 1-[(Trialkylsilyl)-methyl]propenamides." Synlett 2011, no. 13 (2011): 1888–94. http://dx.doi.org/10.1055/s-0030-1260960.

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10

Kharas, Gregory B., Benjamin L. Hill, Vida M. Gaizutis, et al. "Novel Copolymers of Styrene. 3. Oxy Ring-disubstituted 2-cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 50, no. 6 (2013): 575–80. http://dx.doi.org/10.1080/10601325.2013.784166.

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11

Kharas, Gregory B., Benjamin L. Hill, Christopher H. Agos, et al. "Novel Copolymers of Styrene. 2. Oxy Ring-Substituted 2-Cyano-3-phenyl 2-propenamides." Journal of Macromolecular Science, Part A 50, no. 8 (2013): 797–802. http://dx.doi.org/10.1080/10601325.2013.801758.

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12

Kharas, Gregory B., Emi Hanawa, Aida B. Agpasa, et al. "Novel copolymers of styrene. 1. Alkyl ring-substituted 2-cyano-3-phenyl 2-propenamides." Polymer Bulletin 70, no. 2 (2012): 707–14. http://dx.doi.org/10.1007/s00289-012-0838-3.

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13

Kharas, G. B., Nathan J. Kuffel, Thomas Speltz, et al. "Novel Copolymers of Styrene. 4. Halophenoxy Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 1 (2014): 10–14. http://dx.doi.org/10.1080/10601325.2014.976743.

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14

Kharas, Gregory B., Deborah M. De Boer, Miranda E. Fellows, et al. "Novel Copolymers of Styrene. 5. Some Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 1 (2014): 15–19. http://dx.doi.org/10.1080/10601325.2014.976744.

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15

Kharas, G. B., Hemal Bhavsar, Kylie S. Nordness, et al. "Novel Copolymers of Styrene. 10. Halo Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 6 (2015): 407–11. http://dx.doi.org/10.1080/10601325.2015.1029364.

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16

Kharas, Gregory B., Lawrence J. Kray, Sansi L. Mitchell, et al. "Novel Copolymers of Styrene. 6. Halogen Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 2 (2015): 85–89. http://dx.doi.org/10.1080/10601325.2015.980711.

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17

Kharas, Gregory B., Lisa M. Gennett, Yolondria L. Harvey, et al. "Novel Copolymers of Styrene. 7. Chlorine Ring-Substituted 2-Cyano-3-phenyl-2-propenamides." Journal of Macromolecular Science, Part A 52, no. 3 (2015): 163–67. http://dx.doi.org/10.1080/10601325.2015.996935.

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18

Tanaka, Kazuhiko, Hidemi Yoda, Yutaka Isobe, and Aritsune Kaji. "Asymmetric synthesis of .alpha.-methylene-.gamma.-butyrolactones using chiral N-monosubstituted 2-[(tributylstannyl)methyl]propenamides." Journal of Organic Chemistry 51, no. 10 (1986): 1856–66. http://dx.doi.org/10.1021/jo00360a038.

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19

Li, Yue H., Frank T. Coppo, Karen A. Evans, et al. "Synthesis and structure–activity relationships of 3-phenyl-2-propenamides as inhibitors of glycogen phosphorylase a." Bioorganic & Medicinal Chemistry Letters 16, no. 22 (2006): 5892–96. http://dx.doi.org/10.1016/j.bmcl.2006.08.055.

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20

Kharas, Gregory B., William S. Schjerven, Raymond Wenk, et al. "Novel Copolymers of Styrene. 9. Methyl and Methoxy Ring-Substituted 2-Cyano-3-phenyl 2-propenamides." Journal of Macromolecular Science, Part A 52, no. 5 (2015): 360–64. http://dx.doi.org/10.1080/10601325.2015.1018806.

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21

Kharas, Gregory B., Kristen E. McColough, Jeffrey R. Heiskell, et al. "Synthesis and copolymerization of ring-substituted N-(aminocarbonyl)-2-cyano-3-phenyl-2-propenamides with styrene." Designed Monomers and Polymers 6, no. 1 (2003): 103–13. http://dx.doi.org/10.1163/156855503321127574.

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22

Dassonville, Alexandra, Morgane Lardic, Anne Breteche, et al. "N-Pyridinyl(methyl)-indole-1- or 3-propanamides and propenamides acting as topical and systemic inflammation inhibitors." Journal of Enzyme Inhibition and Medicinal Chemistry 23, no. 5 (2008): 728–38. http://dx.doi.org/10.1080/14756360802208251.

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23

Kharas, Gregory B., Xue Tian, Adam C. Hermsen, et al. "Novel Copolymers of Styrene and Alkoxy Ring‐Substituted 2‐Cyano‐N,N‐Dimethyl‐3‐Phenyl‐2‐Propenamides." Journal of Macromolecular Science, Part A 43, no. 10 (2006): 1485–92. http://dx.doi.org/10.1080/10601320600896520.

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24

Kharas, Gregory B., Xue Tian, Whitney K. Castle, et al. "Novel Copolymers of Styrene and Alkyl Ring‐Substituted 2‐Cyano‐N,N‐dimethyl‐3‐phenyl‐2‐propenamides." Journal of Macromolecular Science, Part A 44, no. 1 (2007): 1–5. http://dx.doi.org/10.1080/10601320601041761.

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25

Kharas, Gregory B., Xue Tian, Traci A. Ackron, et al. "Novel Copolymers of Styrene and Halogen Ring‐Substituted 2‐Cyano‐N,N‐Dimethyl‐3‐Phenyl‐2‐Propenamides." Journal of Macromolecular Science, Part A 44, no. 3 (2007): 243–47. http://dx.doi.org/10.1080/10601320601076981.

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26

Kharas, Gregory B., Xue Tian, Whitney K. Castle, et al. "Novel Copolymers of Styrene and Some Ring‐Substituted 2‐Cyano‐N,N‐Dimethyl‐3‐Phenyl‐2‐Propenamides." Journal of Macromolecular Science, Part A 44, no. 4 (2007): 355–58. http://dx.doi.org/10.1080/10601320601187978.

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27

Kharas, Gregory B., Xue Tian, Trang H. Huynh, et al. "Novel Copolymers of Styrene and Halogen Ring‐Disubstituted 2‐Cyano‐N,N‐Dimethyl‐3‐Phenyl‐2‐Propenamides." Journal of Macromolecular Science, Part A 44, no. 5 (2007): 469–73. http://dx.doi.org/10.1080/10601320701228961.

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28

Kharas, Gregory B., Xue Tian, Joanna Alegarbes, et al. "Novel Copolymers of Styrene and Some Ring‐Substituted 2‐Cyano‐N,N‐Dimethyl‐3‐Phenyl‐2‐Propenamides." Journal of Macromolecular Science, Part A 44, no. 6 (2007): 565–68. http://dx.doi.org/10.1080/10601320701283529.

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29

Lewis, Frederick D., Charlotte L. Stern, and Beth A. Yoon. "Effects of inter- and intramolecular hydrogen bonding upon the structure and photoisomerization of 3-(2-pyridyl)propenamides." Journal of the American Chemical Society 114, no. 8 (1992): 3131–33. http://dx.doi.org/10.1021/ja00034a066.

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30

Tanaka, Kazuhiko, Hidemi Yoda, Yutaka Isobe та Aritsune Kaji. "Asymmetric synthesis of γ-alkayl-α-methylene-γ-butyrolactones via 1,6-remote induction using 2-[(tributylstannyl) methyl]propenamides". Tetrahedron Letters 26, № 10 (1985): 1337–40. http://dx.doi.org/10.1016/s0040-4039(00)94887-1.

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31

Lewis, Frederick D., and Beth A. Yoon. "The Influence of Inter- and Intramolecular Hydrogen Bonding upon the Structure and Photochemistry of 3-(2-Pyridyl)propenamides." Journal of Organic Chemistry 59, no. 9 (1994): 2537–45. http://dx.doi.org/10.1021/jo00088a040.

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32

Neel, Kamal, and W. Bhagwat V. "QSAR study of novel inhibitors of human histone deacetylase with in vivo antitumor activity." Journal of Indian Chemical Society Vol. 87, Dec 2010 (2010): 1563–70. https://doi.org/10.5281/zenodo.5805148.

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School of Studies in Chemistry & Biochemistry, Vikram University, Ujjain-456 010, Madhya Pradesh. India <em>E-mail:</em> neelkamalchem@gmail.com Prashanti College of Engineering, Ujjain, Madhya Pradesh. India <em>E-mail:</em> inf_vw@rediffmail.com <em>Manuscript received 12 October 2010, accepted 27 October 2010</em> The paper describe modeling of log IC<sub>50 </sub>representing<em> in vivo</em> antitumor activity using chemical as well as topological descriptors. The results hove shown that the chemical descriptors ore no useful for modeling of the antitumor activity. However, topologica

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33

Kharas, Gregory B., Xue Tian, Stephen P. Denson, et al. "Novel Copolymers of Styrene and Di‐ and Trimethoxy Ring‐Substituted 2‐Cyano‐N,N‐dimethyl‐3‐phenyl‐2‐propenamides." Journal of Macromolecular Science, Part A 44, no. 2 (2007): 125–29. http://dx.doi.org/10.1080/10601320601030632.

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34

Massa, Silvio, Antonello Mai, Gianluca Sbardella, et al. "3-(4-Aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a New Class of Synthetic Histone Deacetylase Inhibitors." Journal of Medicinal Chemistry 44, no. 13 (2001): 2069–72. http://dx.doi.org/10.1021/jm015515v.

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35

LEWIS, F. D., C. L. STERN, and B. A. YOON. "ChemInform Abstract: Effects of Inter- and Intramolecular Hydrogen Bonding Upon the Structure and Photoisomerization of 3-(2-Pyridyl)propenamides." ChemInform 23, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199232086.

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36

Kim, Dae-Kee, Ju Young Lee, Jae-Sun Kim, et al. "Synthesis and Biological Evaluation of 3-(4-Substituted-phenyl)-N-hydroxy-2-propenamides, a New Class of Histone Deacetylase Inhibitors." Journal of Medicinal Chemistry 46, no. 26 (2003): 5745–51. http://dx.doi.org/10.1021/jm030377q.

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37

Anh, Duong T., Nguyen T. Thuan, Pham-The Hai, et al. "Design, Synthesis and Evaluation of Novel 3/4-((Substituted benzamidophenoxy) methyl)-N-hydroxybenzamides/propenamides as Histone Deacetylase Inhibitors and Antitumor Agents." Anti-Cancer Agents in Medicinal Chemistry 19, no. 4 (2019): 546–56. http://dx.doi.org/10.2174/1871520618666181114113347.

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Background: Histone Deacetylase (HDAC) inhibitors represent an extensive class of targeted anticancer agents. Among the most explored structure moieties, hydroxybenzamides and hydroxypropenamides have been demonstrated to have potential HDAC inhibitory effects. Several compounds of these structural classes have been approved for clinical uses to treat different types of cancer, such as givinostat (ITF2357) and belinostat (PXD-101). Aims: This study aims at developing novel HDAC inhibitors bearing N-hydroxybenzamides and Nhydroxypropenamides scaffolds with potential cytotoxicity against differe

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38

Kobayashi, Kazuhiro, Kenichi Hashimoto, Taiyo Shiokawa, Osamu Morikawa, and Hisatoshi Konishi. "Synthesis of (Z)-2-(2H-Isoquinolin-1-ylidene)acetamides by Iodine-Mediated Cyclization of (Z)-3-Amino-3-(2-vinylphenyl)propenamides." Synthesis 2007, no. 6 (2007): 824–28. http://dx.doi.org/10.1055/s-2007-965934.

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39

Urdaneta, Neudo A., José Salazar, Julio C. Herrera, and Simón E. López. "A Facile Synthesis of (E,Z)‐3‐Chloro‐2‐propenamides, Acids, and Esters from 2,3‐Acetylenic Acids with Oxalyl Chloride in DMF." Synthetic Communications 34, no. 4 (2004): 657–64. http://dx.doi.org/10.1081/scc-120027713.

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40

Remiszewski, Stacy W., Lidia C. Sambucetti, Kenneth W. Bair, et al. "N-Hydroxy-3-phenyl-2-propenamides as Novel Inhibitors of Human Histone Deacetylase with in Vivo Antitumor Activity: Discovery of (2E)-N-Hydroxy-3-[4-[[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824)." Journal of Medicinal Chemistry 46, no. 21 (2003): 4609–24. http://dx.doi.org/10.1021/jm030235w.

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41

Alharbi, Osama, Wael H. Alsaedi, Mosa Alsehli, et al. "Novel Quinoline- and Naphthalene-Incorporated Hydrazineylidene–Propenamide Analogues as Antidiabetic Agents: Design, Synthesis, and Computational Studies." Pharmaceuticals 17, no. 12 (2024): 1692. https://doi.org/10.3390/ph17121692.

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Background: Type 2 diabetes has become a significant global health challenge. Numerous drugs have been developed to treat the condition, either as standalone therapies or in combination when glycemic control cannot be achieved with a single medication. As existing treatments often come with limitations, there is an increasing focus on creating novel therapeutic agents that offer greater efficacy and fewer side effects to better address this widespread issue. Methods: The methylene derivatives 3a,b were coupled with phenyl/ethyl isothiocyanate in the basic medium, and dimethyl sulfate was subse

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42

Johnson, WM, SW Littler, and CR Strauss. "Structural Revision and Synthesis of Sinharine and Methylsinharine." Australian Journal of Chemistry 47, no. 4 (1994): 751. http://dx.doi.org/10.1071/ch9940751.

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An unambiguous synthesis of the published structure for the natural product sinharine (1) showed that the assignment was incorrect. (E)-3-( Methylthio )-N-(2-phenylethyl) propenamide (4) was proposed as an alternative structure and this was confirmed by synthesis. Similarly the literature proposal for the structure of methylsinharine was reviewed and the natural product tentatively reassigned as (E)-N-methyl-3-( methylthio )-N-(2-phenylethyl) propenamide.

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43

Chen, Chung-Yi, Yu-Ting Yeh, and Woei-Ling Yang. "Amides from the Stem of Capsicum annuum." Natural Product Communications 6, no. 2 (2011): 1934578X1100600. http://dx.doi.org/10.1177/1934578x1100600217.

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7′-(4′-hydroxyphenyl)- N-[(4-methoxyphenyl)ethyl]propenamide (1), 7′-(3′,4′-dihydroxyphenyl)- N-[(4-methoxyphenyl)ethyl]propenamide (2), N-p-trans-coumaroyltyramine (3), N-trans-caffeoyltyramine (4), β-sitostenone (5), ferulic acid (6), hydroferulic acid (7), 5-hydroxy-3,4-dimethoxycinnamic acid (8), veratic acid (9), vanillic acid (10), isovanillic acid (11), syringic acid (12), (+)-syringaresinol (13), and pheophorbide a (14) were isolated from the stems of Capsicum annuum (Solanaceae). Among them, 1 is a new amide compound. The structures of these compounds were characterized and identified

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44

Mai, Antonello, Silvio Massa, Ilaria Cerbara, et al. "3-(4-Aroyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 2. Effect of Pyrrole-C2and/or -C4Substitutions on Biological Activity†." Journal of Medicinal Chemistry 47, no. 5 (2004): 1098–109. http://dx.doi.org/10.1021/jm030990+.

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45

Shan, Chaoyue, Yongle Huang, and Yu Wang. "Design and Synthesis of Polyacrylamide Quaternary Ammonium Salt with Antibacterial Activity." Journal of Physics: Conference Series 2713, no. 1 (2024): 012027. http://dx.doi.org/10.1088/1742-6596/2713/1/012027.

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Abstract Propenamine quaternary ammonium salt (NNDBAB) containing unsaturated bonds was synthesized from propenamine and bromobutane by alkylation reaction. Using NNDBAB as a monomer, PNNDBAB was further self-polymerized by free radical polymerization to produce propenamine quaternary ammonium salt (PNNDBAB). The structure of NNDBAB was characterized by infrared spectroscopy and nuclear magnetic resonance spectroscopy. The antibacterial properties of PNNDBAB were characterized by an antibacterial zone test, minimum inhibitory concentration, and smear plate counting. The results showed that PNN

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46

Li, Xiong, Ya Zhao, Song Huang, et al. "New Dihydrochalcone and Propenamide from Lithocarpus polystachyus." Natural Product Communications 9, no. 5 (2014): 1934578X1400900. http://dx.doi.org/10.1177/1934578x1400900516.

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Two new compounds, (E)-4-(3, 4-dihydroxyphenyl)-N-(1-hydroxy-2-(4-hydroxyphenyl) ethyl)-2-oxobut-3-enamide (1) and phloretin2-O-β-D-apiofuranosyl (1→6)-β-D-glucopyranoside (2) were isolated from Lithocarpus polystachyus Rehd. Their structures were determined on the basis of analysis of their 1D and 2D NMR spectroscopic and mass spectral data.

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47

Ragno, Rino, Antonello Mai, Silvio Massa та ін. "3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 3. Discovery of Novel Lead Compounds through Structure-Based Drug Design and Docking Studies†,Δ". Journal of Medicinal Chemistry 47, № 6 (2004): 1351–59. http://dx.doi.org/10.1021/jm031036f.

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48

Zhang, Dan, Laura E. Harrington, Hiroo Tanaka, and Robert Pelton. "[3-(Propenamido)phenyl]boronic acid." Acta Crystallographica Section E Structure Reports Online 63, no. 12 (2007): o4628. http://dx.doi.org/10.1107/s1600536807055389.

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49

Sobechko, Iryna, Yana Chetverzhuk, Yuri Horak, Valentyn Serheyev, Victoriia Kochubei, and Nadiia Velychkivska. "THERMODYNAMIC PROPERTIES OF 2-CYANO-3-[5-(PHENYL)-2-FURYL]-2-PROPENAMIDE AND 2-CYANO-3-[5-(4-METHYLPHENYL)-2-FURYL]-2-PROPENAMIDE SOLUTIONS IN ORGANIC SOLVENTS." Chemistry & Chemical Technology 11, no. 2 (2017): 131–37. http://dx.doi.org/10.23939/chcht11.02.131.

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50

Dorosh, A. K., N. M. Bilko, and D. I. Bilko. "Elastic-viscous properties of acrylic acid 2-propenamide gel." Physics of aerodisperse systems, no. 59 (November 8, 2021): 79–88. http://dx.doi.org/10.18524/0367-1631.2021.59.227124.

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The rheological properties of the gel-like material, the monomer of which is a crosslinked and modified 2-propenamide of acrylic acid, were determined by relaxation rheometry methods. The values of its elastic modulus and modulus of losses and complex viscosity depending on: deforming stress and its frequency are determined; relative deformation; temperature in the range (20-100) ° C and the regularities of these dependences are noted. It is established that: 1) the dependence of the modulus of elasticity (G'); modulus of loss (G'') and complex viscosity from: relative deformation; voltage; te

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