Relevant bibliographies by topics / Hydrazino benzothiazoles

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Hydrazino benzothiazoles'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Hydrazino benzothiazoles.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "Hydrazino benzothiazoles"

1

Renu, B. Ghayalkar, and P. Deshmukh Shirish. "Synthesis and antimicrobial activity of 1-naphthyl-2-hydrazino-1,3-benzothiazolylcarbamide." Journal of Indian Chemical Society Vol. 91, Feb 2014 (2014): 305–8. https://doi.org/10.5281/zenodo.5749148.

Full text
Abstract:
Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : renughayalkar@gmail.com <em>Manuscript received online 14 March 2013, revised 19 April 2013, accepted 22 April 2013</em> Seven novel 1-naphthyl-2-hydrazino-1,3-benzothiazolylcarbamides were synthesised by interacting 1-naphthyl isocyanate and various 2-hydrazino-1,3-benzothiazoles. The identities of these newly synthesised carbamides have been established on the basis of usual chemical transformations and<strong> </strong>IR, <sup>1</sup>H NMR and Mass spectral studies and screened for their poss
APA, Harvard, Vancouver, ISO, and other styles
2

Heda, Kavita. M. "Newly synthesized compounds from 2- hydrazino benzothiazole: Characterization, and evaluation of their antibacterial potential." International Journal of Advance and Applied Research 5, no. 23 (2024): 291–94. https://doi.org/10.5281/zenodo.13622529.

Full text
Abstract:
Abstract:Serial of 1-tetra-O-benzoyl-&beta;-D-glucosyl-3-(2)-hydrazino-1, 3-substituted benzothiozolyl thiocarbamide has been synthesized by the interaction &nbsp;of &nbsp; two pharmocophores, &nbsp;tetra-O-benzoyl-&beta;-D-glucosyl isothiocyanates and amine substituted 2-hydrazino-1,3-benzothiazoles in acetone medium. The reaction mixture was kept at room temp for 24 hrs. In acetone medium. Acetone is evaporated then product is recrystallised by petroleum ether (60-80%). &nbsp;Benz-fused compounds have been employed in the synthesis of various compounds which show very potential pharmacologic
APA, Harvard, Vancouver, ISO, and other styles
3

K. Jassim, Ibtisam, Sawsan S. Harth, Rua M. Dhedan, and Ali Obais Abd. "Synthesis and study the biological activity of some six, five and fused ring heteroatome systems derived from 2-mercapto benzothiazole." Tikrit Journal of Pharmaceutical Sciences 8, no. 1 (2023): 96–105. http://dx.doi.org/10.25130/tjphs.2012.8.1.12.96.105.

Full text
Abstract:
In this paper ,new series of 2-hydrazino benzothiazole [1], 2-N-benzothiazole-N`-phenyl hydrazine carboxamide [2], 2-N-[(3)-N`-phenyl-5-(p-bromophenyl)-2`-hydroxy-1,3-oxazolin-2`-yl] benzothiazol hydrazine [3] , 2-N-benzothiazole-N`-1-naphthyl hydrazine carboxamide [4], 2-N-[(3`)-N`-(1-naphthyl)-5`-(p-bromo phenyl)-2`-hydroxy-1,3-oxazolin-2`-yl)] benzothiazol hydrazine [5], of 2-thiaacetic acid benzothiazole [6] ,2-thiaacetyl chloride benzothiazole [7], 5-amino-2-mercapto-1,3,4-thiadiazole [8], of 2-mercapto-[5-acetamid thiamethyl benzothiazol]-1,3,4-thiadiazole [9], 2-phenyl-5-chloromethyl-1,
APA, Harvard, Vancouver, ISO, and other styles
4

SHARMA, K. "ChemInform Abstract: Chemistry of 2-Hydrazinobenzazoles (2-Hydrazino-benzimidazoles Benzothiazoles and Benzoxazoles)." ChemInform 26, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199526281.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Sharma, Neetesh Kumar, and Raghvendra Singh Bhadauria. "Synthesis and Biological Evaluation of 1-(6-bromobenzo [d]thiazol-2-yl)-2-(disubstituted methylene) hydrazine derivatives." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 577–86. http://dx.doi.org/10.22270/jddt.v9i4-a.3520.

Full text
Abstract:
Synthesis of a series of various 1-(6-bromobenzo[d]thiazol-2-yl)-2-(disubstitutedmethylene)hydrazine derivatives (7a-7e)have been done. Synthesis of a series of intermediates (3 and 5) have been also done, 6-bromo-1,3-benzothiazole-2-amine (3), 2-hydrazino-6-bromo-1, 3-benzothiazole (5) and final product (7a-7e), 1-(6-bromobenzo[d]thiazol-2-yl)-2-(diphenylmethylene) hydrazine (7a), 1-(6-bromobenzo [d]thiazol-2-yl)-2-(propan-2-ylidene) hydrazine (7b), (E)-2-(butan-2-ylidene)-1-(6-bromobenzo[d]thiazol-2-yl)hydrazine (7c), (Z)-1-(6-bromobenzo[d]thiazol-2-yl)-2-(cyclohexylmethylene) hydrazine (7d)
APA, Harvard, Vancouver, ISO, and other styles
6

Sharma, Neetesh Kumar, and Raghvendra Singh Bhadauria. "Synthesis and Biological Evaluation of 1-(6-chlorobenzo [d]thiazol-2-yl)-2-(disubstituted methylene) hydrazine derivatives." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 561–72. http://dx.doi.org/10.22270/jddt.v9i4-a.3515.

Full text
Abstract:
Synthesis of a series of various 1-(6-chlorobenzo[d]thiazol-2-yl)-2-(disubstitutedmethylene)hydrazine derivatives (7a-7e)have been done. Synthesis of a series of intermediates (3 and 5) have been also done, 6-Chloro-2-amine-1,3-benzothiazole (3), 2-hydrazino-6-chloro-1, 3-benzothiazole (5) and final product (7a-7e), 1-(6-chlorobenzo[d]thiazol-2-yl)-2-(diphenylmethylene) hydrazine (7a), 1-(6-chlorobenzo [d]thiazol-2-yl)-2-(propan-2-ylidene) hydrazine (7b), (E)-2-(butan-2-ylidene)-1-(6-chlorobenzo[d]thiazol-2-yl)hydrazine (7c), (Z)-1-(6-chlorobenzo[d]thiazol-2-yl)-2-(cyclohexylmethylene) hydrazi
APA, Harvard, Vancouver, ISO, and other styles
7

Bhat, M., S. L. Belagali, N. K. H. Kumar, and S. Jagannath. "Anti-mitotic Activity of the Benzothiazole-pyrazole Hybrid Derivatives." Anti-Infective Agents 17, no. 1 (2018): 66–73. http://dx.doi.org/10.2174/2211352516666180914101758.

Full text
Abstract:
Background: Nitrogen-containing heterocyclics are abundant in natural products and also in synthetic drug molecules because of a variety of applications and superior pharmacological profile action. Pyrazoles are the integral architects of many of the heterocyclic compounds with superior biological activity. Methods: Two series of the pyrazole conjugated Benzothiazole derivatives were synthesized. The pyrazoles were synthesized by the Vilsmeier-Haack reaction and then conjugated with benzothiazole hydrazine and hydrazide by imine bond formation. The synthesized compounds were screened for anti-
APA, Harvard, Vancouver, ISO, and other styles
8

Lamkane, Rachana B., Priyanka M. Khadasare, Pooja M. Shinde, et al. "Synthesis and Biological Screening of Novel Derivatives of Benzothiazol as Anticonvulsant Agents." SAR Journal of Medical Biochemistry 4, no. 01 (2023): 6–15. http://dx.doi.org/10.36346/sarjmb.2023.v04i01.002.

Full text
Abstract:
The Benzothiazole ring system belongs to a much studied class of compound. In the last few decades, the chemistry of benzothiazole and their fused heterocyclic derivatives have received considerable attention owing to their significant and effective biological activity. The present study aimed to design and synthesize novel derivatives of bezothiazole obtained from 3-chloro-4-flouro aniline treated with potassium thiocynide with chloro acetyl chloride gives (7-chloro-6-fluro-1,3-benzothiazol-2-yl) acetyl chloride which is converted into hydrazide and yields the resultant compound derivatives o
APA, Harvard, Vancouver, ISO, and other styles
9

Morscher, Alexandra, Marcus V. N. de Souza, James L. Wardell, and William T. A. Harrison. "Expected and unexpected products of reactions of 2-hydrazinylbenzothiazole with 3-nitrobenzenesulfonyl chloride in different solvents." Acta Crystallographica Section E Crystallographic Communications 74, no. 5 (2018): 673–77. http://dx.doi.org/10.1107/s2056989018005595.

Full text
Abstract:
The syntheses and crystal structures of 2-[2-(propan-2-ylidene)hydrazinyl]-1,3-benzothiazol-3-ium 3-nitrobenzenesulfonate (C10H12N2S+·C6H4NO5S−), (I), 2-[2-(3-nitrobenzenesulfonyl)hydrazinyl]-1,3-benzothiazole (C13H10N4O4S2), (II) and 2-[2-(3-nitrobenzenesulfonyl)hydrazinyl]-1,3-benzothiazol-3-ium 3-nitrobenzenesulfonate (C13H11N4O4S2 +·C6H4NO5S−), (III) are reported. Salt (I) arose from an unexpected reaction of 2-hydrazinylbenzothiazole with the acetone solvent in the presence of 3-nitrobenzenesulfonyl chloride, whereas (II) and (III) were recovered from the equivalent reaction carried out i
APA, Harvard, Vancouver, ISO, and other styles
10

S.V, Mamatha, S. L. Belagali, and Mahesh Bhat. "Synthesis and SAR Evaluation of Mercapto Triazolobenzothiazole." Anti-Infective Agents 18, no. 4 (2021): 362–74. http://dx.doi.org/10.2174/2211352517666191204095558.

Full text
Abstract:
Background: Benzothiazoles possess a vast sphere of biological activities including anti- inflammatory, antibacterial activities whereas triazoles display various pharmacological properties including antimicrobial and antitubercular activities. Hence, triazole conjugated benzothiazole side-chain anticipating their interesting biological properties has been focused upon. Objective: The objective of the current work is synthesis and biological evaluation of a new series of benzothiazole appended triazole derivatives. Methods: The target compounds were prepared via a multi-step method involving t
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "Hydrazino benzothiazoles"

1

Chung, Ching-Hui, and 鍾景揮. "(A) Synthesis of Aryl Hydrazide via Sonochemical Barbier-type Reaction and (B) Microwave Assisted Synthesis of Benzothiazole by Reaction of 2-Aminothiophenol with Aldehyde and Carboxylic Acid." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/52799365776440710530.

Full text
Abstract:
碩士<br>淡江大學<br>化學學系碩士班<br>95<br>Aryl hydrazides are important precursors for synthesis of a variety of heterocycles such as indoles, pyrazoles, β-lactams, quinazolines and others, they are well known to be biologically active. In addition, aryl hydrazides can be transformed to aryl hydrazines and aryl amines, which can be further applied to synthesize heterocyclic compounds. Herein, our laboratory wish to report a novel synthetic method for preparation of aryl hydrazide from arylbromide, magnesium powder, 1,2-dibromoethane and diethyl azodicarboxylate via sonochemical Barbier-type reaction. In
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "Hydrazino benzothiazoles"

1

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of trichloro[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]iron(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_413.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of trichloro[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]- chromium(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_99.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of triacetato[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]iron(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_404.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of triacetato[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]- chromium(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_98.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of trinitrato[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]- chromium(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_104.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of trinitrato[N-(3-methyl-1-thiocarbamyl-5-oxo-2-pyrazolin-4-ylene)-N′-(4′-benzothiazole)-hydrazine]iron(III)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_415.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'Hydrazino benzothiazoles' for particular source types:
Journal articles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography