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2,4-Pentadien-1-one, 1-(4-chlorophenyl)-5-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62643-84-9

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62643-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62643-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,4 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62643-84:
(7*6)+(6*2)+(5*6)+(4*4)+(3*3)+(2*8)+(1*4)=129
129 % 10 = 9
So 62643-84-9 is a valid CAS Registry Number.

62643-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-5-(4-methylphenyl)penta-2,4-dien-1-one

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:62643-84-9 SDS

62643-84-9Downstream Products

62643-84-9Relevant academic research and scientific papers

Lewis Acid-Mediated Ring-Opening Reactions of trans-2-Aroyl-3-styrylcyclopropane-1,1-dicarboxylates: Access to Cyclopentenes and E,E-1,3-Dienes

Thangamani, Murugesan,Srinivasan, Kannupal

, p. 571 - 577 (2018)

The ring-opening reaction of trans-2-aroyl-3-styrylcyclopropane-1,1-dicarboxylates was investigated with different Lewis acids. With SnCl4, the cyclopropane dicarboxylates afforded cyclopentene derivatives through ring opening followed by cyclization (vinylcyclopropane-cyclopentene rearrangement). With TiCl4, they furnished E,E-1,3-diene derivatives stereoselectively via ring opening followed by proton elimination.

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