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1,3-Benzenedicarbonyl dichloride, 5-(4-bromophenoxy)-, also known as 5-(4-bromophenoxy)isophthalonitrile, is an organic compound with the chemical formula C14H7BrN2O2. It is a white to off-white crystalline solid that is soluble in organic solvents. 1,3-Benzenedicarbonyl dichloride, 5-(4-bromophenoxy)- is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is characterized by its aromatic structure, featuring a benzene ring with two carbonyl groups at the 1 and 3 positions, and a 4-bromophenoxy group attached at the 5 position. The presence of the bromine atom and the nitrile groups make it a valuable building block for the creation of more complex molecules in the chemical industry.

92675-05-3

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92675-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92675-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,7 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92675-05:
(7*9)+(6*2)+(5*6)+(4*7)+(3*5)+(2*0)+(1*5)=153
153 % 10 = 3
So 92675-05-3 is a valid CAS Registry Number.

92675-05-3SDS

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 5-(4-bromophenoxy)benzene-1,3-dicarbonyl chloride

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

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More Details:92675-05-3 SDS

92675-05-3Upstream product

92675-05-3Relevant academic research and scientific papers

5-(4-ethynylophenoxy)isophthalic chloride

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, (2008/06/13)

Sulfone-ester polymers containing pendent ethynyl groups and a direct and multi-step process for preparing same are disclosed. The multi-step process involves the conversion of a pendent bromo group to the ethynyl group while the direct route involves rea

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