Academic literature on the topic '2-Chlorobenzonitrile'

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Journal articles on the topic "2-Chlorobenzonitrile"

1

B., Hari Babu, Venkateswara Rao K. T., Suh Y. W., Sai Prasad P. S., and Lingaiah N. "One-step selective synthesis of 2-chlorobenzonitrile from 2-chlorotoluene via ammoxidation." New Journal of Chemistry 42, no. 3 (2018): 1892–901. http://dx.doi.org/10.1039/c7nj03728g.

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Isolated and polymeric vanadia formulate V<sub>2</sub>O<sub>5</sub>/Al<sub>2</sub>O<sub>3</sub> catalysts selective for the synthesis of 2-chlorobenzonitrile from 2-chlorotoluene in a single step through ammoxidation.
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2

Onda, Masao, Masahiro Sakuma, Tatsuji Shimoe, Noriyuki Saegusa, and Ichiro Yamaguchi. "Microwave spectrum and quadrupole coupling constant of 2-chlorobenzonitrile." Journal of Molecular Structure 323 (July 1994): 287–88. http://dx.doi.org/10.1016/0022-2860(94)08311-8.

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3

Aim, Karel. "A modified ebulliometric method for high-boiling substances: vapour pressures of 2-chlorobenzonitrile and 4-chlorobenzonitrile at temperatures from 380 K to 490 K." Journal of Chemical Thermodynamics 26, no. 9 (1994): 977–86. http://dx.doi.org/10.1006/jcht.1994.1115.

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4

Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Ragini Singh, and Snehasis Jana. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.5281/zenodo.35219.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi&rsquo;s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric
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5

Trivedi, Mahendra Kumar, Alice Branton, Dahryn Trivedi, Gopal Nayak, Ragini Singh, and Snehasis Jana. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.5281/zenodo.186726.

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2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi&rsquo;s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric
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6

Buronov, A., A. Nasrullaev, Kh Bozorov, N. Lifei, and H. A. Aisa. "NEW TETRACYCLIC THIENO[3,2-d]PYRIMIDINE SCAFFOLD DERIVATIVES SYNTHESIZED AND AMINATED." 2022-yil 3-son (133/1) ANIQ FANLAR SERIYASI 1, no. 1 (2025): 12–17. https://doi.org/10.59251/2181-1296.2025.v1.149.2.3208.

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The synthesis of novel thieno[3,2-d]pyrimidine derivatives started with the reaction of 5-bromo-2 chlorobenzonitrile with ethyl-2-mercaptoacetate to give the compound AT-2. The addition of lactames to the formed AT-2 followed by cyclization gave the compound AR-05. The amination reaction was then used to facilitate the formation of a C-C bond. The intermediate AR-05 was formed under a base in dioxane in the presence of aromatic amines and a palladium catalyst, forming a new nitrogen-carbon bond. AR-58-1 and AR-82 were synthesized as end products. The structure of the new compounds was studied
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7

Buronov, A., A. Nasrullaev, Kh Bozorov, N. Lifei, S. Kulmirzaeva, and A. Ishankulov. "SYNTHESIS OF NOVEL TETRACYCLIC THIENO[3,2-d]PYRIMIDINONES." 2022-yil 3-son (133/1) ANIQ FANLAR SERIYASI 1, no. 1 (2025): 5–11. https://doi.org/10.59251/2181-1296.2025.v1.149.2.3206.

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The synthesis of novel thieno[3,2-d]pyrimidine derivatives commenced with 5-bromo-2-chlorobenzonitrile with ethyl-2-mercaptoacetate, which yielded the compound AT-2. The addition of piperidin-2-one to the formed AT-2 and subsequent cyclization yielded the compound AR-05. Subsequently, the Suzuki cross-coupling reaction was employed to facilitate the formation of a carbon-carbon bond. The intermediate AR-05 was formed in an alkaline medium in a toluene/water mixture in the presence of arylboronic acid and a palladium catalyst, forming a new C-C bond. AR-27 was synthesized as the final product.
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8

Mahendra, Kumar Trivedi, Branton Alice, Nayak Gopal, and Trivedi Dahryn. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38–46. https://doi.org/10.11648/j.mc.20150304.11.

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Abstract:
2-chlorobenzonitrile (2-ClBN) is widely used in the manufacturing of azo dyes, pharmaceuticals, and as intermediate in various chemical reactions. The aim of present study was to evaluate the impact of biofield treatment on physical, thermal and spectroscopic properties of 2-ClBN. 2-ClBN sample was divided into two groups that served as treated and control. The treated group received Mr. Trivedi&rsquo;s biofield treatment. Subsequently, the control and treated samples were evaluated using X-ray diffraction (XRD), surface area analyser, differential scanning calorimetry (DSC), thermogravimetric
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9

Kumar Trivedi, Mahendra. "Experimental Investigation on Physical, Thermal and Spectroscopic Properties of 2-Chlorobenzonitrile: Impact of Biofield Treatment." Modern Chemistry 3, no. 4 (2015): 38. http://dx.doi.org/10.11648/j.mc.20150304.11.

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10

Sudha, S., N. Sundaraganesan, M. Kurt, M. Cinar, and M. Karabacak. "FT-IR and FT-Raman spectra, vibrational assignments, NBO analysis and DFT calculations of 2-amino-4-chlorobenzonitrile." Journal of Molecular Structure 985, no. 2-3 (2011): 148–56. http://dx.doi.org/10.1016/j.molstruc.2010.10.035.

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