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153172-70-4

N-(2-cyanophenyl)-3-methylbenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 153172-70-4 Structure

  • Basic information

    1. Product Name: N-(2-cyanophenyl)-3-methylbenzamide
    2. Synonyms: N-(2-cyanophenyl)-3-methylbenzamide
    3. CAS NO:153172-70-4
    4. Molecular Formula: C15H12N2O
    5. Molecular Weight: 236.26858
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 153172-70-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(2-cyanophenyl)-3-methylbenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-cyanophenyl)-3-methylbenzamide(153172-70-4)
    11. EPA Substance Registry System: N-(2-cyanophenyl)-3-methylbenzamide(153172-70-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 153172-70-4(Hazardous Substances Data)

153172-70-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153172-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,7 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153172-70:
(8*1)+(7*5)+(6*3)+(5*1)+(4*7)+(3*2)+(2*7)+(1*0)=114
114 % 10 = 4
So 153172-70-4 is a valid CAS Registry Number.

153172-70-4Relevant articles and documents

Acyl Cyanides as Bifunctional Reagent: Application in Copper-Catalyzed Cyanoamidation and Cyanoesterification Reaction

Chen, Zhengwang,Wen, Xiaowei,Zheng, Weiping,He, Ruolan,Chen, Dou,Cao, Dingsheng,Long, Lipeng,Ye, Min

, p. 5691 - 5701 (2020/04/10)

Cu-catalyzed domino decyanation and cyanation reaction of acyl cyanides with amines or alcohols have been developed. The cyano sources were generated in situ via C-CN cleavage yielding the corresponding cyano substituted amides or esters in moderate to excellent yields. This approach features a cheap copper catalyst, domino decyanation and cyanation reaction, readily available starting materials, broad substrate scope, operational simplicity, and the potential for further transformation of the cyano group.

Pd-Catalyzed tandem reaction of N-(2-cyanoaryl)benzamides with arylboronic acids: synthesis of quinazolines

Zhu, Jianghe,Shao, Yinlin,Hu, Kun,Qi, Linjun,Cheng, Tianxing,Chen, Jiuxi

supporting information, p. 8596 - 8603 (2018/11/27)

The synthesis of 2,4-disubstituted quinazolines by a palladium-catalyzed reaction of arylboronic acids with N-(2-cyanoaryl)benzamides has been developed with moderate to excellent yields. The method shows good functional group tolerance. In particular, ha

Synthesis of 2-Aminobenzonitriles through Nitrosation Reaction and Sequential Iron(III)-Catalyzed C-C Bond Cleavage of 2-Arylindoles

Chen, Wei-Li,Wu, Si-Yi,Mo, Xue-Ling,Wei, Liu-Xu,Liang, Cui,Mo, Dong-Liang

, p. 3527 - 3530 (2018/06/26)

A variety of 2-aminobenzonitriles were prepared from 2-arylindoles in good to excellent yields through tert-butylnitrite (TBN)-mediated nitrosation and sequential iron(III)-catalyzed C-C Bond cleavage in a one-pot fashion. The 2-aminobenzonitriles can be used to rapidly synthesize benzoxazinones by intramolecular condensation. The present method features an inexpensive iron(III) catalyst, gram scalable preparations, and novel C-C bond cleavage of indoles.

Anchimeric Assistance in the Specific Acid-catalyzed Hydration of Benzonitriles

Smyth, Richard M.,Williams, Andrew

, p. 2171 - 2174 (2007/10/02)

2-(Acylamido)benzonitriles react to give exclusively the corresponding 2-(acylamido)benzamides under relatively mild aqueous acid conditions.The kinetics for hydration at 50 deg C in aqueous HCl with ionic strength kept at 1 mol dm-3 with KCl o

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