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3-methyl-2-(2H-1,2,3-triazol-2-yl)benzonitrile is a chemical compound with the molecular formula C11H8N4. It is a derivative of benzonitrile, featuring a methyl group at the 3rd carbon and a 2H-1,2,3-triazol-2-yl group at the 2nd carbon. 3-methyl-2-(2H-1,2,3-triazol-2-yl)benzonitrile is known for its potential applications in various chemical and pharmaceutical industries, particularly as a building block for the synthesis of more complex molecules. Its structure provides a unique combination of aromatic, heterocyclic, and nitrile functionalities, which can be exploited in the design of new compounds with specific properties. The compound's reactivity and stability make it a valuable intermediate in organic synthesis, and its properties can be further explored for the development of new materials or pharmaceuticals.

1293285-64-9

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1293285-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1293285-64-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,3,2,8 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1293285-64:
(9*1)+(8*2)+(7*9)+(6*3)+(5*2)+(4*8)+(3*5)+(2*6)+(1*4)=179
179 % 10 = 9
So 1293285-64-9 is a valid CAS Registry Number.

1293285-64-9Relevant academic research and scientific papers

Rhodium-Catalyzed ortho-Cyanation of 2-Aryl-1,2,3-triazole: An Alternative Approach to Suvorexant

Zhang, Hailong,Jing, Li,Zheng, Yang,Sang, Rui,Zhao, Yi,Wang, Qiantao,Wu, Yong

supporting information, p. 723 - 729 (2018/02/21)

A rhodium-catalyzed ortho-cyanation protocol for 2-aryl-1,2,3-triazole has been developed by using N-cyano-N-phenyl-p-toluensulfonamide (NCTS) as an environmentally friendly cyanide source. This simple cyanation reaction provides a new protocol for the diversification of benzonitriles in moderate to good yields and tolerates useful functional groups. In addition, the method was used to synthesize 5-methyl-2-(2H-1,2,3-triazol-2-yl)benzoic acid, which is the key intermediate of suvorexant.

2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Paragraph 0441; 0442, (2015/06/17)

The present invention relates to 2-(1,2,3-triazol-2-yl)benzamide and 3-(1,2,3-triazol-2-yl)picolinamide derivatives of formula (I) wherein Ar1, Q, and R1 to R5 are as described in the description, to their preparation, to

2-(1,2,3-TRIAZOL-2-YL)BENZAMIDE AND 3-(1,2,3-TRIAZOL-2-YL)PICOLINAMIDE DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 59, (2013/05/23)

The present invention relates to 2-(1,2,3-triazol-2-yl)benzamide and 3-(1,2,3-triazol-2- yl)picolinamide derivatives of formula (I) Formula (I) wherein Ar1, Q, and R1 to R5 are as described in the description, to their pre

DISUBSTITUTED OCTAHY-DROPYRROLO [3,4-C] PYRROLES AS OREXIN RECEPTOR MODULATORS

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Page/Page column 89, (2012/11/07)

Disubstituted octahydropyrrolo[3,4-c]pyrrole compounds are described, which are useful as orexin receptor modulators. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

FUSED HETEROCYCLIC COMPOUNDS AS OREXIN RECEPTOR MODULATORS

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Page/Page column 67-68, (2011/05/06)

Disubstituted 3,8-diaza-bicyclo[4.2.0]octane and 3,6-diazabicyclo [3.2.0]heptane compounds are described, which are useful as orexin receptor modulators. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

FUSED HETEROCYCLIC COMPOUNDS AS OREXIN RECEPTOR MODULATORS

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Page/Page column 62-63, (2011/05/06)

Certain disubstituted 3,8-diaza-bicyclo[4.2.0]octane and 3,6-diazabicyclo [3.2.0]heptane are described, which are useful as orexin inhibitors. Such compounds may be useful in pharmaceutical compositions and methods for the treatment of diseased states, disorders, and conditions mediated by orexin activity, such as insomnia.

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