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952-03-4

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952-03-4 Usage

General Description

3-Methyl-3'-nitro-1,1'-biphenyl is a chemical compound with the molecular formula C13H11NO2. It is a nitro derivative of biphenyl, with a methyl group attached to the third carbon and a nitro group attached to the third carbon of the second benzene ring. 3-Methyl-3'-nitro-1,1'-biphenyl is commonly used in the synthesis of various organic compounds and pharmaceutical products. It is a pale yellow solid with a melting point of 105-107 °C and is considered to be potentially hazardous due to its irritant and toxic properties. 3-Methyl-3'-nitro-1,1'-biphenyl is primarily used in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 952-03-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,5 and 2 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 952-03:
(5*9)+(4*5)+(3*2)+(2*0)+(1*3)=74
74 % 10 = 4
So 952-03-4 is a valid CAS Registry Number.

952-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Methyl-3'-nitro-1,1'-biphenyl

1.2 Other means of identification

Product number -
Other names 1-methyl-3-(3-nitrophenyl)benzene

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:952-03-4 SDS

952-03-4Relevant articles and documents

New synthesis of biaryls via Rh-catalyzed decarbonylative Suzuki-coupling of carboxylic anhydrides with arylboroxines

Goossen,Paetzold

, p. 1665 - 1668 (2007/10/03)

The catalytic cross-coupling of aromatic carboxylic anhydrides or acid chlorides with triarylboroxines has been achieved for the first time under decarbonylation, giving rise to the unsymmetrical biaryls rather than the expected diaryl ketones. This new decarbonylative Suzuki coupling, catalyzed by a [Rh(ethylene)2Cl]2/KF system, can be applied to aromatic, heteroaromatic and vinylic carboxylic anhydrides, potentially opening up new perspectives for the use of carboxylic acid derivatives as substrates in biaryl syntheses.

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