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Cyclooctanone, 5-phenyl-, also known as 5-phenylcyclooctan-1-one, is an organic compound with the molecular formula C15H18O. It is a cyclic ketone with a phenyl group attached to the fifth carbon of the cyclooctane ring. Cyclooctanone, 5-phenyl- is characterized by its unique molecular structure, which consists of an eight-membered carbon ring with a carbonyl group (C=O) and a benzene ring attached to it. Cyclooctanone, 5-phenyl-, is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile chemical properties and reactivity. It can be synthesized through various methods, such as the Friedel-Crafts acylation of cyclooctene with benzoyl chloride or the condensation of cyclooctanone with benzylmagnesium chloride. The compound is typically used as a building block in the preparation of more complex molecules and has potential applications in the development of new drugs and materials.

833-51-2

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833-51-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 833-51-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 3 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 833-51:
(5*8)+(4*3)+(3*3)+(2*5)+(1*1)=72
72 % 10 = 2
So 833-51-2 is a valid CAS Registry Number.

833-51-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenylcyclooctan-1-one

1.2 Other means of identification

Product number -
Other names Cyclooctanone,5-phenyl

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:833-51-2 SDS

833-51-2Relevant academic research and scientific papers

Regioselective radical ring-opening reaction of bicyclo[4.2.0]octan-2-ones promoted by samarium(II) iodide

Kakiuchi, Kiyomi,Minato, Koichi,Tsutsumi, Ken,Morimoto, Tsumoru,Kurosawa, Hideo

, p. 1963 - 1966 (2007/10/03)

Radical ring-opening reactions of bicyclo[4.2.0]octanones, its C6 alkyl derivatives, and tricyclic ketones promoted by SmI2 gave cyclohexanones via fission of the external cyclobutane bond. The CO2Me, CN, and phenyl derivatives led t

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