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2-ethyl-1-phenylbutane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39581-96-9

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39581-96-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39581-96-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,8 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39581-96:
(7*3)+(6*9)+(5*5)+(4*8)+(3*1)+(2*9)+(1*6)=159
159 % 10 = 9
So 39581-96-9 is a valid CAS Registry Number.

39581-96-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-1-phenylbutane-1,3-dione

1.2 Other means of identification

Product number -
Other names 2-ethyl-1-phenyl-1,3-butanedione

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:39581-96-9 SDS

39581-96-9Relevant academic research and scientific papers

Palladium(II)- and platinum(II)-catalyzed addition of stabilized carbon nucleophiles to ethylene and propylene

Wang, Xiang,Widenhoefer, Ross A.

, p. 660 - 661 (2004)

PdCl2(CH3CN)2 and [PtCl2(H 2C=CH2)]2 catalyze the addition of β-dicarbonyl compounds to ethylene and propylene.

Rhodium promoted isomerisation of allylic alkoxides: A new method for enolate anion formation

Gazzard, Lewis J.,Motherwell, William B.,Sandham, David A.

, p. 979 - 993 (2007/10/03)

Transition metal mediated isomerisation of allylic alkoxides is presented as a new method for enolate anion generation. The scope and limitations of enolate formation with the catalysts [Rh(dppe)(THF)2]+ClO4- and (Ph3P)3RhCl are explored and the synthetic potential of the methodology demonstrated in the stereoselective formation and reactions of certain ketone and aldehyde enolates.

TRAPPING REACTION OF ENOLATES FROM LITHIUM DIMETHYLCUPRATE CONJUGATED ADDITION: IMPORTANCE OF STERIC FACTORS AND, PARTICULARLY, OF β-SUBSTITUTION OF ENONE IN THE C- vs. O-ACYLATION

Bernasconi, Silvana,Jommi, Giancarlo,Montanari, Stefania,Sisti, Massimo

, p. 125 - 128 (2007/10/02)

Conjugated addition of lithium dimethylcuprate to α,β-unsaturated ketones gives intermediate enolates which, treated with acetyl chloride, undergo O- and/or C-acylation depending on the substitution at the enone β-carbon.Results agree with the hypothesis that C-acylation proceeds through an intramolecular metal-assisted mechanism.

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