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4-Thiazoleacetic acid, 2-[(phenylsulfonyl)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62557-35-1

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62557-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62557-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62557-35:
(7*6)+(6*2)+(5*5)+(4*5)+(3*7)+(2*3)+(1*5)=131
131 % 10 = 1
So 62557-35-1 is a valid CAS Registry Number.

62557-35-1SDS

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 ethyl 2-[2-(benzenesulfonamido)-1,3-thiazol-4-yl]acetate

1.2 Other means of identification

Product number -
Other names 2-phenylsulfonylamino-1,3-thiazol-4-yl-acetic acid ethyl ester

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:62557-35-1 SDS

62557-35-1Relevant academic research and scientific papers

New 2-amino-thiazole-4-acetamides with antiplatelet activity

Rehse, Klaus,Baselt, Tobias

experimental part, p. 645 - 654 (2009/04/06)

In the Born test, 23 title compounds were synthesized and investigated for their antiplatelet activities against collagen, ADP, adrenaline, and platelet-activating factor (PAF) as inducers of the aggregation. Using collagen, three compounds with IC50 values below 10 μM were found (3a, 3b, 3c) and 15 compounds with IC50 values between 10 and 100 μM were determined. In general, a cyclohexylamino rest on an 4-carboxamide moiety is a pre-requisite for this pharmacological activity. A clear dependence from the substituent R1 in the structural element Y is observed. The same is true for the spacer n in the 4-carboxamide substituent. Compound 3e showed strong ADP-antagonistic effects (IC50 = 2.2 nM); 3c antagonized adrenaline (IC50 = 2.8 nM), while 3n was highly effective against platelet-activating factor (IC50 = 0.2 μM).

3-Substituted-7-substituted alkanamido-3-cephem-4-carboxylic acid compounds

-

, (2008/06/13)

3-Substituted-7-substituted alkanamido-3-cephem-4-carboxylic acid compounds and pharmaceutically acceptable salts thereof which have antimicrobial activities, processes for the preparation thereof, pharmaceutical compositions comprising the same, and meth

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