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2-Cyclopenten-1-one, 2-(4-chlorophenyl)-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87506-06-7

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87506-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87506-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,0 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87506-06:
(7*8)+(6*7)+(5*5)+(4*0)+(3*6)+(2*0)+(1*6)=147
147 % 10 = 7
So 87506-06-7 is a valid CAS Registry Number.

87506-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)-3-methylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Cyclopenten-1-one,2-(4-chlorophenyl)-3-methyl

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:87506-06-7 SDS

87506-06-7Downstream Products

87506-06-7Relevant academic research and scientific papers

Catalytic intermolecular Pauson-Khand-type reaction: Strong directing effect of pyridylsilyl and pyrimidylsilyl groups and isolation of Ru complexes relevant to catalytic reaction

Itami, Kenichiro,Mitsudo, Koichi,Fujita, Kazuyoshi,Ohashi, Youichi,Yoshida, Jun-Ichi

, p. 11058 - 11066 (2007/10/03)

Some circumstantial evidence for the directing effect of the 2-pyhdylsilyl group in the Ru-catalyzed intermolecular Pauson-Khand-type reaction (PKR) of alkenyl(2-pyridyl)silane, alkyne, and carbon monoxide has been provided. Most importantly, we have succeeded in isolating several monometallic Ru complexes relevant to the catalytic reaction: Ru(vinylsilane)(CO)3 complexes and ruthenacyclopentene. While the stoichimetric reaction of the Ru(vinylsilane)(CO)3 complex with an alkyne led to the formation of the corresponding cyclopentenone (PKR product) at 100 °C, the ruthenacyclopentene intermediate was quantitatively produced at 50 °C. This complex was also converted to a cyclopentenone upon heating at 100 °C. Moreover, it was also found that the Ru(vinylsilane)(CO)3 complex and ruthenacyclopentene serve as catalysts in intermolecular PKR.

Ring Expansion of Succinoin Derivatives. New Synthetic Routes to Cyclopentenones

Nakamura, Eiichi,Shimada, Jun-ichi,Kuwajima, Isao

, p. 498 - 499 (2007/10/02)

Acid-catalysed ring expansion reactions of cyclobutane derivatives bearing a vicinal substituted-diol group give α-aryl and α-vinyl substituted cyclopentenones in good yields.

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