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141563-05-5

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141563-05-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141563-05-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,5,6 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141563-05:
(8*1)+(7*4)+(6*1)+(5*5)+(4*6)+(3*3)+(2*0)+(1*5)=105
105 % 10 = 5
So 141563-05-5 is a valid CAS Registry Number.

141563-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-2-Amino-1,2-dicyanovinyl]imidoformic hydrazide

1.2 Other means of identification

Product number -
Other names 2-amino-3-hydroxy-N-[2-methoxy-5-[2-(3,4,5-trimethoxyphenyl)ethenyl]phenyl]propanamide hydrochloride

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:141563-05-5 SDS

141563-05-5Relevant articles and documents

(Z)-N3-(2-Amino-1,2-dicyanovinyl)formamidrazone: a Precursor in the Synthesis of 1,5-Diaminoimidazoles and 6-Carbamoyl-1,2-dihydropurines

Alves, M. Jose,Booth, Brian L.,Freitas, A. Paula,Proenca, M. Fernanda J. R. P.

, p. 913 - 917 (2007/10/02)

The reaction of ethyl (Z)-N-(2-amino-1,2-dicyanovinyl)formimidate with hydrazine monohydrate leads to (Z)-N3-(2-amino-1,2-dicyanovinyl)formamidrazone in almost quantitative yield.This compound proved to be an important starting material for the synthesis of the corresponding N1-isopropylidene- and N1-acetyl-formamidrazones.The amidrazones prepared promptly cyclize in the presence of base to give a 1,5-diamino-4-cyanoimidazole or a 1,5-diamino-4-(cyanoformimidoyl)imidazole, depending on the reaction conditions and mainly on the nature of the base used to induce cyclization. 1,5-Diamino-4-(cyanoformimidoyl)imidazole was treated with carbonyl compounds and the 1,2-dihydropurines thus isolated indicated that the amino group in position 5 is more reactive than that in position 1.

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