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88073-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88073-36-3 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 88073-36:
(7*8)+(6*8)+(5*0)+(4*7)+(3*3)+(2*3)+(1*6)=153
153 % 10 = 3
So 88073-36-3 is a valid CAS Registry Number.

88073-36-3SDS

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-1-phenyl-2-pentene-1,4-dione

1.2 Other means of identification

Product number	-
Other names	3-benzoyl-1-phenyl-pent-2t-ene-1,4-dione

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:88073-36-3 SDS

88073-36-3Upstream product

88073-36-3Downstream Products

88073-36-3Relevant articles and documents

Stereoselective synthesis of α-ylidene-β-dicarbonyl compounds: A mild PhI(OAc)2-mediated dehydrogenation process

Fan, Liyan,Chen, Wen,Tang, Kunshan,Wu, Dongbei

, p. 940 - 942 (2012/11/06)

PhI(OAc)2-mediated dehydrogenation of α-alkyl-β-dicarbonyl compound has been developed to afford α-ylidene-β- dicarbonyl compounds with high stereoselectivity under mild conditions. This process provides a complementary entry to stereoselectivity for the Knoevenagel reaction.

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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88073-36-3