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68827-52-1

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68827-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68827-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,8,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68827-52:
(7*6)+(6*8)+(5*8)+(4*2)+(3*7)+(2*5)+(1*2)=171
171 % 10 = 1
So 68827-52-1 is a valid CAS Registry Number.

68827-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 7-oxo-2-phenyl-7H-[1,2,4]triazolo[3,2-b][1,3]thiazine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Phenyl-7-carbomethoxy-s-triazolo[3,2-b]-1,3-thiazin-5-on

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:68827-52-1 SDS

68827-52-1Relevant articles and documents

One step synthesis of highly functionalized thiazolo[3,2-b][1,2,4]triazole, triazolo[1,5-a]pyrimidine and triazolo[3,4-b][1,3,4]thiadiazine

Shah, Tariq A.,Ahmad, Zubair,Mir, Niyaz A.,Muneer,Rath, Nigam P.,Ahmad, Musheer

, p. 107931 - 107937 (2015)

An efficient and straightforward methodology for the preparation of novel functionalized thiazolo[3,2-b]triazole, triazolo[1,5-a]pyrimidine and triazolo[3,4-b][1,3,4]thiadiazine has been implemented with excellent yields via a one-pot catalyst-free proced

Synthesis and transformations of 5-substituted 2-aryl-7H-[1,2,4]triazolo[3, 2-b][1,3]thiazin-7-ones and 2-aryl-2,3-dihydro-4H-[1,3]thiazino[3,2-a] benzimidazol-4-ones

Britsun,Esipenko,Chernega,Lozinskii

, p. 108 - 113 (2007/10/03)

3-Aryl-1,2,4-triazole-5-thiones react with dimethyl acetylenedicarboxylate and methyl 3-phenyl-propynoate to afford the corresponding 5-substituted 2-aryl-7H-[1,2,4]triazolo[3,2-b][1,3]thiazin-7-ones. Treatment of 2-aryl-2,3-dihydro-4H-[1,3]thiazino[3,2-a]benzimidazol-4-ones with alkalies leads to formation of 3-(benzimidazol-2-ylsulfanyl)-3-arylpropionic acids, their reaction with methyl p-toluenesulfonate yields 1-(3-methyl-2-thioxo-2,3- dihydro-1N-benzimidazol-1-yl)-3-phenyl-2-propen-1-one, and oxidation with hydrogen peroxide gives benzimidazole-2-sulfonic acid and 3-aryl-2-propenoic acids. 2005 Pleiades Publishing, Inc.

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