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53824-23-0

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53824-23-0 Usage

Chemical class

Biphenyl

Substitution

Chloro-substituted

Position of methoxy group

2-position of one of the phenyl rings

Applications

a. Manufacture of pharmaceuticals
b. Agrochemicals
c. Production of dyes and pigments
d. Intermediate in the synthesis of other organic compounds

Potential uses

Medicinal chemistry

Structural features

May contribute to its potential applications in medicinal chemistry

Health and environmental risks

Requires careful handling to avoid hazards and risks

Management

Proper handling and disposal are necessary to minimize health and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 53824-23-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,2 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53824-23:
(7*5)+(6*3)+(5*8)+(4*2)+(3*4)+(2*2)+(1*3)=120
120 % 10 = 0
So 53824-23-0 is a valid CAS Registry Number.

53824-23-0SDS

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 1-chloro-4-(2-methoxyphenyl)benzene

1.2 Other means of identification

Product number -
Other names (4'-chloro-biphenyl-2-yl)-methyl ether

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:53824-23-0 SDS

53824-23-0Relevant articles and documents

A general synthesis of diarylketones by means of a three-component cross-coupling of aryl and heteroaryl bromides, carbon monoxide, and boronic acids

Neumann, Helfried,Brennfuehrer, Anne,Beller, Matthias

experimental part, p. 3645 - 3652 (2009/04/11)

Pd(OAc)2/di-1-adamantyl-n-butylphosphine (cataCXium A) is highly active in the three-component Suzuki carbonylation and represents the most general catalyst system reported up to now. A broad range of aryl/heteroaryl bromides and aryl boronic acids can be coupled to the corresponding diarylketones at low catalyst loadings.

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