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3,4-bis(4-chlorophenyl)cyclopentanone, also known as 3,4-Dichlorophenylcyclopentanone or DCPC, is a synthetic chemical compound with the molecular formula C15H14Cl2O. It is a white crystalline solid that is soluble in organic solvents and has a melting point of approximately 150-152°C. DCPC is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential health and environmental risks, it is important to handle and dispose of 3,4-bis(4-chlorophenyl)cyclopentanone with proper safety measures and regulations.

1772-51-6

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1772-51-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1772-51-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,7 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1772-51:
(6*1)+(5*7)+(4*7)+(3*2)+(2*5)+(1*1)=86
86 % 10 = 6
So 1772-51-6 is a valid CAS Registry Number.

1772-51-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-bis(4-chlorophenyl)cyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 3,4-Bis-<4-chlor-phenyl>-cyclopentanon

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:1772-51-6 SDS

1772-51-6Upstream product

1772-51-6Downstream Products

1772-51-6Relevant academic research and scientific papers

Oxidatively initiated NHC-catalyzed enantioselective synthesis of 3,4-disubstituted cyclopentanones from enals

White, Nicholas A.,Rovis, Tomislav

supporting information, p. 10112 - 10115 (2015/09/01)

An unprecedented N-heterocyclic carbene (NHC)-catalyzed annulation of enals to form 3,4-disubstituted cyclopentanones has been discovered. Aryl enals undergo dimerization in the presence of a single-electron oxidant to form C2 symmetric cyclopentanones. A cross-reaction has also been developed, allowing for the synthesis of differentially substituted cyclopentanones. Mechanistically, the reaction is thought to proceed through radical intermediates, further establishing the synthetic utility of this class of reactivity.

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