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73728-78-6

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73728-78-6 Usage

Molecular class

Biphenylamines

Structure

Two benzene rings linked by a single carbon-carbon bond

Substitution

Four methyl groups at the 2', 3', 4', and 6' positions on the biphenyl ring

Functional group

Amine group at the 4 position

Usage

Building block for the synthesis of various organic compounds in organic synthesis and pharmaceutical research

Potential

Biological activities, research tool in medicinal chemistry and drug discovery

Check Digit Verification of cas no

The CAS Registry Mumber 73728-78-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,7,2 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73728-78:
(7*7)+(6*3)+(5*7)+(4*2)+(3*8)+(2*7)+(1*8)=156
156 % 10 = 6
So 73728-78-6 is a valid CAS Registry Number.

73728-78-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4-(2,4,6-trimethylphenyl)aniline

1.2 Other means of identification

Product number -
Other names 3,2',4',6'-Tetramethylbiphenylamine

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:73728-78-6 SDS

73728-78-6Downstream Products

73728-78-6Relevant articles and documents

Metal-free synthesis of sterically crowded biphenyls by direct Ar-H substitution in alkyl benzenes

Dichiarante, Valentina,Fagnoni, Maurizio,Albini, Angelo

, p. 6495 - 6498 (2008/09/16)

(Chemical Equation Presented) Four's definitely a crowd: The chemoselective activation of Ar-H bonds in methylbenzenes by treatment with photogenerated phenyl cations allowed the synthesis of sterically crowded biphenyl compounds, including tetra-ortho-substituted biphenyls, by intermolecular cross-coupling (see scheme). This method is an appealing metal-free alternative to widely used transition-metal catalysis. TFE = 2,2,2-trifluoroethanol.

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