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1,3-Butanedione, 1-(4-ethenylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53498-48-9

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53498-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53498-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,9 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53498-48:
(7*5)+(6*3)+(5*4)+(4*9)+(3*8)+(2*4)+(1*8)=149
149 % 10 = 9
So 53498-48-9 is a valid CAS Registry Number.

53498-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-ethenylphenyl)butane-1,3-dione

1.2 Other means of identification

Product number -
Other names 1,3-Butanedione,1-(4-ethenylphenyl)

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:53498-48-9 SDS

53498-48-9Downstream Products

53498-48-9Relevant academic research and scientific papers

Process for preparing vinyl substituted beta-diketones

-

Page/Page column 6-7, (2008/06/13)

A process for preparing vinyl substituted beta-diketones includes reacting a halogen-containing beta-diketone with an olefin in a reaction zone under Heck coupling reaction conditions in the presence of a catalyst, a base, and an organic phosphine to provide a vinyl substituted beta-diketone product.

Synthesis of vinyl-substituted β-diketones for polymerizable metal complexes

Southard, Glen E.,Murray, George M.

, p. 9036 - 9039 (2007/10/03)

Polymerizable β-diketones for application to metal ion coordination have been prepared and characterized. Bromine-substituted β-diketones were synthesized under Claisen-Schmidt-type condensation conditions. Vinyl groups were substituted for the halide by

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