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ethyl (2-phenyl[1,3]thiazolo[3,2-b][1,2,4]triazol-6-yl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66870-63-1

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66870-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66870-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66870-63:
(7*6)+(6*6)+(5*8)+(4*7)+(3*0)+(2*6)+(1*3)=161
161 % 10 = 1
So 66870-63-1 is a valid CAS Registry Number.

66870-63-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(2-phenyl-[1,3]thiazolo[3,2-b][1,2,4]triazol-6-yl)acetate

1.2 Other means of identification

Product number -
Other names HMS1450P04

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:66870-63-1 SDS

66870-63-1Relevant academic research and scientific papers

Design and synthesis of some thiazolotriazolyl esters as anti-inflammatory and analgesic agents

Tozkoparan, Birsen,Aytac, S. Peri,Guersoy, Sule,Aktay, Goeknur

, p. 192 - 201 (2012/09/08)

In order to develop potent analgesic/antiinflammatory compounds with reduced ulcerogenic risk, a series of thiazolotriazolyl-carboxylic and acetic acid esters were synthesized and characterized by spectral and elementary analysis. All synthesized compounds were screened for in vivo anti-inflammatory activities in mice by carregeenan-induced paw edema model. The compounds showing 20% reduction in paw edema were also evaluated for their analgesic activities by acetic acid-induced writhing test and the gastric ulceration risk by determining the lipid peroxidation level in stomachs. Among the compounds tested, compounds 1, 4, 6, 7, 8, 1a, 2a, 3a, 4a, 7a, 2b, and 8b showed moderate-to-good anti-inflammatory activity at various doses in any of the measurement intervals. Compounds 7a, 2b, and 8b were the most actives of the series in analgesic activity test. Moreover, compounds 1, 4, and 8 were found to be safe in stomach in respect of free radical production. Springer Science+Business Media, LLC 2010.

Sur la synthese d'acides thiazolotriazolylacetiques

Moskowitz, H.,Mignot, A.,Miocque, M.

, p. 1321 - 1323 (2007/10/02)

During the synthesis of thiazolotriazolylacetic acids, the condensation of ethyl 4-chloro-3-oxobutyrate with triazolinethiones was studied.The use of an alkaline reagent (triethylamine) leads only to S-alkylation and not to the expected cyclized product.T

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