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2,5-diphenylcyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73331-36-9

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73331-36-9 Usage

General Description

2,5-diphenylcyclopentanone is a compound that belongs to the ketone family, characterized by a cyclopentanone ring with two phenyl groups attached at the 2 and 5 positions. It is a white crystalline solid at room temperature and has a molecular formula of C17H16O. 2,5-diphenylcyclopentanone is often used as a precursor in organic synthesis and is known for its role in the preparation of various pharmaceuticals and fine chemicals. Its unique structure and reactivity make it a valuable building block for the creation of complex organic molecules in the field of medicinal chemistry and drug discovery. Additionally, it has potential applications in materials science and as a reagent in laboratory research.

Check Digit Verification of cas no

The CAS Registry Mumber 73331-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,3,3 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73331-36:
(7*7)+(6*3)+(5*3)+(4*3)+(3*1)+(2*3)+(1*6)=109
109 % 10 = 9
So 73331-36-9 is a valid CAS Registry Number.

73331-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-diphenylcyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2,5-diphenyl-cyclopentanone

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:73331-36-9 SDS

73331-36-9Relevant academic research and scientific papers

Carbonylation of Enynes under Hydroformylation Conditions Catalyzed by Rhodium Carbonyl. A New Method for Synthesis of Cyclic Enones

Doyama, Kazuo,Joh, Takashi,Shiohara, Tomoo,Takahashi, Shigetoshi

, p. 4353 - 4360 (2007/10/02)

The reactivities of 1-buten-3-yne derivatives toward hydroformylation were studied using a rhodium catalyst.Unexpectedly, cyclopentenone derivatives were obtained in moderate yields together with formyl-substituted dienes and unsaturated lactones.This rea

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