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1,1'-Biphenyl, 3-chloro-3'-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19482-18-9

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19482-18-9 Usage

Family

Biphenyl

Structure

Two benzene rings connected by a single bond with a chlorine atom and a methyl group attached

Appearance

Pale yellow solid at room temperature

Uses

Production of various organic and pharmaceutical compounds, potential applications in materials science and organic synthesis

Safety

Should be handled and stored with care to prevent hazards to human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 19482-18-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19482-18:
(7*1)+(6*9)+(5*4)+(4*8)+(3*2)+(2*1)+(1*8)=129
129 % 10 = 9
So 19482-18-9 is a valid CAS Registry Number.

19482-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-3'-methyl-1,1'-biphenyl

1.2 Other means of identification

Product number -
Other names -

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:19482-18-9 SDS

19482-18-9Downstream Products

19482-18-9Relevant academic research and scientific papers

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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