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36715-97-6

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36715-97-6 Usage

General Description

3-Methyl-1,2-benzenedicarbonitrile, also known as 3-Methyl-2,3-diphenylacrylonitrile, is a chemical compound with the molecular formula C10H7N. It is a white solid with a molecular weight of 185.17 g/mol and a melting point of 165-168°C. This organic compound is commonly used in the production of pharmaceuticals, dyes, and other industrial chemicals. It is also used as a building block for the synthesis of various organic compounds. 3-Methyl-1,2-benzenedicarbonitrile is considered to be toxic and may cause irritation to the skin, eyes, and respiratory system upon exposure.

Check Digit Verification of cas no

The CAS Registry Mumber 36715-97-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,1 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 36715-97:
(7*3)+(6*6)+(5*7)+(4*1)+(3*5)+(2*9)+(1*7)=136
136 % 10 = 6
So 36715-97-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N2/c1-7-3-2-4-8(5-10)9(7)6-11/h2-4H,1H3

36715-97-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methylbenzene-1,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 1,2-Benzenedicarbonitrile,3-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:36715-97-6 SDS

36715-97-6Downstream Products

36715-97-6Relevant articles and documents

An easy route from catechols to phthalonitriles

Drechsler, Ulf,Hanack, Michael

, p. 1207 - 1208 (2007/10/03)

An easy synthetic route from substituted catechols via their corresponding aryl bistriflates to substituted phthalonitriles is described. The displacement of the triflate groups in catechol triflates by cyanide ions proceeded in high yields using zinc cyanide and palladium-1,1′-bis(diphenylphosphino)ferrocene as catalyst. The mild reaction conditions tolerate numerous functional groups and represent a desirable alternative to the generally low-yielding Rosenmund-von Braun reaction.

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