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71597-10-9

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71597-10-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71597-10-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71597-10:
(7*7)+(6*1)+(5*5)+(4*9)+(3*7)+(2*1)+(1*0)=139
139 % 10 = 9
So 71597-10-9 is a valid CAS Registry Number.

71597-10-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3,5-dimethoxyphenyl)-1-methyl-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 1H-1,2,4-Triazole,5-(3,5-dimethoxyphenyl)-1-methyl

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:71597-10-9 SDS

71597-10-9Downstream Products

71597-10-9Relevant articles and documents

USE OF ARYL CHLORIDES IN PALLADIUM-CATALYZED C-H BOND FUNCTIONALIZATION

-

Page/Page column 5; 13, (2009/01/24)

A one-step method for efficiently converting carbon-hydrogen bonds into carbon-carbon bonds using chloroarenes and palladium catalysts is disclosed. This method allows faster introduction of complex molecular entities, a process that would otherwise require many more steps. This invention is particularly relevant for the organic synthesis of complex molecules such as, but not limited to, pharmacophores.

Synthesis of 1,2,4-Triazoles and 1,2,4-Oxadiazoles

Lin, Yang-i,Hlavka, Joseph J.,Bitha, Panayoto,Lang, S. A.

, p. 1693 - 1695 (2007/10/02)

Monothiodiacylamines reacted regiospecifically with hydrazines and hydroxylamine to give substituted 1,2,4-triazoles and 1,2,4-oxadiazoles in excellent yields.

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