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1004112-67-7

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1004112-67-7 Usage

General Description

1-Bromo-3-chloro-5-(difluoromethoxy)benzene is a chemical compound with the molecular formula C7H4BrClF2O. It is a colorless liquid with a slightly sweet and fruity odor. 1-Bromo-3-chloro-5-(difluoromethoxy)benzene is mainly used in the production of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as an intermediate in the synthesis of various chemicals. This chemical is not considered to be a significant environmental hazard, but it should still be handled with care due to its potential to cause skin and eye irritation. Overall, 1-Bromo-3-chloro-5-(difluoromethoxy)benzene plays an important role in the production of various chemicals and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1004112-67-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,1,1 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1004112-67:
(9*1)+(8*0)+(7*0)+(6*4)+(5*1)+(4*1)+(3*2)+(2*6)+(1*7)=67
67 % 10 = 7
So 1004112-67-7 is a valid CAS Registry Number.

1004112-67-7SDS

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 1-Bromo-3-chloro-5-(difluoromethoxy)benzene

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:1004112-67-7 SDS

1004112-67-7Downstream Products

1004112-67-7Relevant articles and documents

SYNTHESIS OF DIFLUOROMETHYL ETHERS AND SULFIDES

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Paragraph 00167-00172; 00181-00184, (2014/07/22)

The synthesis of difluoromethyl ethers and sulfides with a simple, non-ozone- depleting reagent is described. The difluoromethylation of phenols with this reagent occurs at room temperature within minutes with exceptional functional group tolerance. The mild conditions makes possible tandem processes for the conversion of aryl boronic acids, aryl halides and arenes to difluoromethyl ethers. Mechanistic studies support a reaction pathway involving nucleophilic attack of the phenolate to difluorocarbene.

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