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2-bromo-4-chloro-3,5-dimethylphenol is an organic compound characterized by its molecular formula C8H8BrClO. It is a derivative of phenol, with a bromine atom at the 2nd carbon, a chlorine atom at the 4th carbon, and two methyl groups at the 3rd and 5th carbons. 2-bromo-4-chloro-3,5-dimethylphenol is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also used as an intermediate in the production of various chemical compounds. The presence of both a bromine and a chlorine atom in the molecule enhances its reactivity and makes it a valuable building block in organic synthesis.

38730-40-4

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38730-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38730-40-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 38730-40:
(7*3)+(6*8)+(5*7)+(4*3)+(3*0)+(2*4)+(1*0)=124
124 % 10 = 4
So 38730-40-4 is a valid CAS Registry Number.

38730-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-4-chloro-3,5-dimethyl-phenol

1.2 Other means of identification

Product number -
Other names 2-Chlor-4-brom-5-hydroxy-m-xylol

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:38730-40-4 SDS

38730-40-4Upstream product

38730-40-4Relevant academic research and scientific papers

Palladium-Catalyzed Enantioselective Synthesis of 2-Aryl Cyclohex-2-enone Atropisomers: Platform Molecules for the Divergent Synthesis of Axially Chiral Biaryl Compounds

Pan, Chongqing,Zhu, Zixi,Zhang, Mingkai,Gu, Zhenhua

supporting information, p. 4777 - 4781 (2017/04/13)

The palladium-catalyzed asymmetric synthesis of enone-based atropisomers from 2-iodo-3-methylcyclohex-2-enones and aryl boronic acid is reported. BoPhoz-type phosphine–aminophosphine ligands showed superior enantioselectivity over other ligands. These cyc

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