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64987-05-9

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64987-05-9 Usage

Uses

Ethyl 2-(2-formylaminothiazol-4-yl) acetate is a reagent used in the synthesis of aryl glyoxylates.

Check Digit Verification of cas no

The CAS Registry Mumber 64987-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,8 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 64987-05:
(7*6)+(6*4)+(5*9)+(4*8)+(3*7)+(2*0)+(1*5)=169
169 % 10 = 9
So 64987-05-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O3S/c1-2-13-7(12)3-6-4-14-8(10-6)9-5-11/h4-5H,2-3H2,1H3,(H,9,10,11)

64987-05-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-(2-formamidothiazol-4-yl)acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-(2-formamido-1,3-thiazol-4-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:64987-05-9 SDS

64987-05-9Relevant articles and documents

Thiazole, imidazole and oxazole compounds and treatments of disorders associated with protein aging

-

, (2008/06/13)

Provided are, among other things, compounds of formula I or IA, . Also provided are methods of treatment with such compounds.

Ring nitrogen functionalization of 2-aminothiazol-4-acetic acid derivatives. I. Synthesis and properties of novel 2-aminothiazole N-oxides

Perrone,Alpegiani,Giudici,et al.

, p. 1097 - 1111 (2007/10/02)

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2-Lower alkyl-7-substituted amino-2 or 3-cephem-4-carboxylic acid compounds

-

, (2008/06/13)

A compound of the formula: STR1 wherein R1 is (C1 to C6) alkyl, R2 is carboxy or a protected carboxy group, R3 is amino or a protected amino group, and A is carbonyl or hydroxy (C1 to C6) alkylene, and pharmaceutically acceptable salt thereof, which is active against pathogenic bacteria, and methods for preparing the same.

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