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Benzene-1,4-diyl bis(4-chlorobenzoate) is a chemical compound with the molecular formula C20H12Cl4O4. It is a white crystalline solid that is formed by the reaction of benzene-1,4-diol with 4-chlorobenzoic acid. benzene-1,4-diyl bis(4-chlorobenzoate) is characterized by its symmetrical structure, with two 4-chlorobenzoate groups attached to a central benzene ring through its 1 and 4 positions. It is known for its potential applications in the synthesis of various organic compounds and as an intermediate in the production of pharmaceuticals and other specialty chemicals. Due to the presence of multiple chlorine atoms, it may also be of interest in the study of halogenated aromatic compounds and their environmental impacts.

5411-00-7

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5411-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5411-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5411-00:
(6*5)+(5*4)+(4*1)+(3*1)+(2*0)+(1*0)=57
57 % 10 = 7
So 5411-00-7 is a valid CAS Registry Number.

5411-00-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-chlorobenzoyl)oxyphenyl] 4-chlorobenzoate

1.2 Other means of identification

Product number -
Other names benzene-1,4-diyl bis(4-chlorobenzoate)

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:5411-00-7 SDS

5411-00-7Downstream Products

5411-00-7Relevant academic research and scientific papers

A new synthetic route to substituted quinones by radical-mediated coupling of organotellurium compounds with quinones

Yamago, Shigeru,Hashidume, Masahiro,Yoshida, Jun-Ichi

, p. 6805 - 6813 (2007/10/03)

Carbon-centered radicals generated from the corresponding organotellurium compounds react with a variety of quinones under photo-thermal conditions to give the monoaddition product in moderate to excellent yield. The reaction can be used for the synthesis of polyprenyl quinoid natural products and C-glycosides.

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