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192933-27-0

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192933-27-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 192933-27-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,9,3 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 192933-27:
(8*1)+(7*9)+(6*2)+(5*9)+(4*3)+(3*3)+(2*2)+(1*7)=160
160 % 10 = 0
So 192933-27-0 is a valid CAS Registry Number.

192933-27-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(N-acetyl-p-cyanoanilino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine, N-acetyl-N-(4-cyanophenyl)-

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:192933-27-0 SDS

192933-27-0Relevant articles and documents

Synthesis of pteridine derivatives related to folic acid and methanopterin from pyrazine-2,3-dicarbonitrile

Tada, Masaru,Asawa, Yasuhiro,Igarashi, Mamoru

, p. 973 - 981 (1997)

Pteridine derivatives related to folic acid and methanopterin were synthesized by two methods. The first synthesis is initiated by the radical substitution of 5-methylpyrazine-2,3-dicarbonitrile (3) with the (N-acyl- anilino)alkyl radical to give 6-methyl-5-(N-acylanilino)alkylpyrazine-2,3- dicarbonitrile (9) and was followed by the substitution of the 2-carbonitrile with methylamine and further conversion to 1 -methyl-2-amino-6-(N- acylanilino)-alkyl-7-methylpteridin-4(1H)-imine 11 by the action of guanidine. The second method is initiated by radical hydroxymethylation of 5- methylpyrazine-2,3-dicarbonitrile (3) to give 5-hydroxymethyl-6- methylpyrazine-2,3-dicarbonitrile (15), followed by oxidation of the hydroxymethyl group, N-phenylimination, and the substitution of the 2- carbonitrile with methylamine to give 6-methyl-2-methyl-amino-5-(N- phenylimino)methenylpyrazine-3-carbonitrile (18). The reduction of the imino group and the final cyclization with guanidine gives 2-amino-6-anilinomethyl- 1,7-dimethylpteridin-4(1H)-imine (20).

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