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Ethanone, 1-(2,3-dibenzoyloxiranyl)-, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88073-34-1

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88073-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88073-34-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,7 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88073-34:
(7*8)+(6*8)+(5*0)+(4*7)+(3*3)+(2*3)+(1*4)=151
151 % 10 = 1
So 88073-34-1 is a valid CAS Registry Number.

88073-34-1SDS

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 3-Benzoyl-2,3-epoxy-1-phenyl-1,4-pentanedione

1.2 Other means of identification

Product number -
Other names -

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:88073-34-1 SDS

88073-34-1Downstream Products

88073-34-1Relevant academic research and scientific papers

Epoxidation of 2-Butene-1,4-diones with Hydrogen Peroxide in the Presence of a Catalytic Amount of Quaternary Ammonium Iodide

Sayama, Shinsei,Inamura, Yutaka

, p. 1993 - 1995 (2007/10/02)

The epoxidation of 1,4-disubstituted 2-butene-1,4-diones with 30percent aq.H2O2 in the presence of a catalytic amount of quaternary ammonium iodide afforded 2,3-epoxy-1,4-butanediones in high yield.

Photosensitized Oxidation of Furans. Part 7. Solvent Effects in Thermal Conversion of the endo-Peroxides of Arylfurans

Graziano, M. Liliana,Iesce, M. Rosaria,Chiosi, Sergio,Scarpati, Rachele

, p. 2071 - 2074 (2007/10/02)

Thermal conversion of the endo-peroxides of the arylfurans (1) in a polar aprotic solvent leads to aroylenol esters (4) and diaroyl epoxides (3), the predominance of one over being concentration dependent.The results can be rationalized on the basis of th

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