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73931-43-8

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73931-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73931-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,3 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73931-43:
(7*7)+(6*3)+(5*9)+(4*3)+(3*1)+(2*4)+(1*3)=138
138 % 10 = 8
So 73931-43-8 is a valid CAS Registry Number.

73931-43-8SDS

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-bromo-1,5-dichloro-3-methoxybenzene

1.2 Other means of identification

Product number -
Other names Benzene,2-bromo-1,5-dichloro-3-methoxy

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:73931-43-8 SDS

73931-43-8Upstream product

73931-43-8Downstream Products

73931-43-8Relevant articles and documents

Synthesis of sterically hindered polychlorinated biphenyl derivatives

Joshi,Vyas,Duffel,Parkin,Lehmler

experimental part, p. 1045 - 1054 (2011/06/20)

A series of sterically hindered (methoxylated) polychlorinated biphenyl derivatives were synthesized using the Suzuki and the Ullmann coupling reactions. The Suzuki coupling with Pd(dba)2-dicyclohexylphosphino-2,6- dimethoxybiphenyl (DPDB) gave better yields (65-98%) compared to the classic Ullmann coupling reaction (20-38%). Despite the reactive catalyst system, no significant coupling with aromatic chlorine substituents was observed. Crystal structure analysis of four PCB derivatives revealed solid state dihedral angles ranging from 69.7 to 81.0, which indicates that these highly ortho-substituted PCB derivatives have some conformational flexibility. Georg Thieme Verlag Stuttgart.

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