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948287-40-9

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948287-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 948287-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,2,8 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 948287-40:
(8*9)+(7*4)+(6*8)+(5*2)+(4*8)+(3*7)+(2*4)+(1*0)=219
219 % 10 = 9
So 948287-40-9 is a valid CAS Registry Number.

948287-40-9SDS

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 5-Thiazoleacetic acid, 2-(phenylamino)-, ethyl ester

1.2 Other means of identification

Product number -
Other names Ethyl 2-(2-(phenylamino)thiazol-5-yl)acetate

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:948287-40-9 SDS

948287-40-9Downstream Products

948287-40-9Relevant articles and documents

Novel one-step method for the conversion of isothiocyanates to 2-alkyl(aryl)aminothiazoles

Sasmal, Pradip K.,Chandrasekhar,Sridhar,Iqbal, Javed

scheme or table, p. 11074 - 11080 (2009/04/11)

2-Aminothiazole derivatives are widely used structural motifs in medicinal chemistry due to their broad application in drug development. Herein we demonstrate a novel one-step method for the synthesis of 2-aminothiazole derivatives from the corresponding isothiocyanates via thiourea formation followed by cycloisomerisation in an intramolecular thia-Michael fashion. This method is very mild, simple and highly efficient and versatile enough to accommodate various amino substitutions at the C2 position of thiazoles. This methodology is equally well applicable to synthesise various 2-substituted amino-5-thiazolylmethylphosphonate derivatives.

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