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62995-73-7

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62995-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62995-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,9 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62995-73:
(7*6)+(6*2)+(5*9)+(4*9)+(3*5)+(2*7)+(1*3)=167
167 % 10 = 7
So 62995-73-7 is a valid CAS Registry Number.

62995-73-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyano-2-methylbenzamide

1.2 Other means of identification

Product number -
Other names BENZAMIDE,N-CYANO-2-METHYL

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62995-73-7 SDS

62995-73-7Downstream Products

62995-73-7Relevant articles and documents

Ultrasound-Assisted Synthesis of N -Acylcyanamides and N -Acyl-Substituted Imidazolones from Carboxylic Acids by Using Trichloroisocyanuric Acid/Triphenylphosphine

Phakhodee, Wong,Yamano, Dolnapa,Pattarawarapan, Mookda

supporting information, p. 703 - 707 (2020/04/08)

A convenient ultrasound-assisted one-pot synthesis of N -acylcyanamides starting from readily available carboxylic acids and sodium cyanamide has been developed. Upon activation in the presence of trichloroisocyanuric acid (TCCA) and triphenylphosphine, a range of carboxylic acids was converted into N -acylcyanamides in good to excellent yields within 10 minutes at room temperature without base. Remarkably, N -acyl-substituted imidazolones were readily accessible through guanylation-cyclization of the in situ generated N -acylcyanamides.

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