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3-Butenoic acid, 3-methyl-2-[[[2-(phenoxymethyl)-4-thiazolyl]carbonyl]amino]-, methyl ester, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61348-77-4

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61348-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61348-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,4 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 61348-77:
(7*6)+(6*1)+(5*3)+(4*4)+(3*8)+(2*7)+(1*7)=124
124 % 10 = 4
So 61348-77-4 is a valid CAS Registry Number.

61348-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-2-[(2-phenoxymethyl-thiazole-4-carbonyl)-amino]-but-3-enoic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

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:61348-77-4 SDS

61348-77-4Downstream Products

61348-77-4Relevant academic research and scientific papers

THE TRAPPING OF SULFENIC ACIDS FROM PENICILLIN SULFOXIDES. ARYL MERCAPTANS

Micetich, Ronald G.,Maiti, Samarendra N.,Tanaka, Motoaki,Yamazaki, Tomio,Ogawa, Kazuo

, p. 1403 - 1409 (2007/10/02)

Aryl mercaptans, unlike heterocyclic mercaptans, reacted exceptionally slowly with penicillin sulfoxides.These reactions are affected by the substituent at the C-6 position of the penam, and by the nature of the ester group at the C-3 position.The unsym- azetidinone disulfides obtained from these reactions, unlike those from heterocyclic mercaptans, did not react with halogenating agents such as cupric chloride.

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