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69022-35-1

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69022-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69022-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,2 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69022-35:
(7*6)+(6*9)+(5*0)+(4*2)+(3*2)+(2*3)+(1*5)=121
121 % 10 = 1
So 69022-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2/c1-6-7(5-9)3-2-4-8(6)10/h2-4H,10H2,1H3

69022-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-2-methylbenzonitrile

1.2 Other means of identification

Product number -
Other names 2-methyl-3-amino-benzonitrile

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:69022-35-1 SDS

69022-35-1Relevant articles and documents

ESTROGEN RECEPTOR MODULATORS AND USES THEREOF

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Paragraph 00493, (2013/10/08)

Described herein are compounds that are estrogen receptor modulators. Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well as methods of using such estrogen receptor modulators, alone and in combination with other compounds, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

Increasing the scope of palladium-catalyzed cyanations of aryl chlorides

Schareina, Thomas,Jackstell, Ralf,Schulz, Thomas,Zapf, Alexander,Cotte, Alain,Gotta, Matthias,Beller, Matthias

experimental part, p. 643 - 648 (2009/11/30)

An improved protocol for the palladium-catalyzed cyanation of electron-rich aryl chlorides with potassium ferrocyanide [K4[Fe(CN)6]] is presented. Compared to previous procedures the substrate scope is significantly broadened.

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