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2-Cyclopenten-1-one, 3-methyl-2,5,5-triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

139722-24-0

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139722-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139722-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,7,2 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 139722-24:
(8*1)+(7*3)+(6*9)+(5*7)+(4*2)+(3*2)+(2*2)+(1*4)=140
140 % 10 = 0
So 139722-24-0 is a valid CAS Registry Number.

139722-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-2,5,5-triphenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-methyl-2,5,5-triphenyl-2-cyclopentenone

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:139722-24-0 SDS

139722-24-0Upstream product

139722-24-0Downstream Products

139722-24-0Relevant academic research and scientific papers

Nonoxidative Transient-Metal-Carbon Bond Cleaving Reactions and Their Application in a Transition-Metal Mediated Cyclopentenone Synthesis.

Ni, LiMing,Belot, John A.,Welker, Mark E.

, p. 177 - 180 (1992)

Cycloaddition reactions of cyclopentadienyl iron dicarbonyl 2-alkynyl complexes (1) with diphenyl ketene (2) yields transition-metal substituted cyclopentenones (4).The transition metals can subsequently be cleaved from the cyclopentenones under a variety of oxidative and nonoxidative reaction conditions.

Reactions of transition-metal η1-allyl and propargyl complexes with ketenes and some new nonoxidative transition-metal-carbon bond cleaving reactions of the ketene cycloadducts which yield cyclopentenones

Stokes, Heather L.,Ni, Li Ming,Belot, John A.,Welker, Mark E.

, p. 95 - 104 (2007/10/02)

Reactions of cyclopentadienyl iron 2-alkynyl and allyl complexes with ketenes or ketene precursors yield transition-metal substituted cyclopentenones in some cases and new transition-metal substituted allyl complexes in others.The transition metals can subsequently be cleaved from the cyclopentenone containing complexes under a variety of oxidative and nonoxidative reaction conditions. Keywords: Iron; Allyl complexes; Alkynyl complexes; Ketenes; Cycloadditions; Cyclopentenones

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