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Pentanoic acid, 3-oxo-2-(phenylmethylene)-, methyl ester, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81734-04-5

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81734-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81734-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,7,3 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81734-04:
(7*8)+(6*1)+(5*7)+(4*3)+(3*4)+(2*0)+(1*4)=125
125 % 10 = 5
So 81734-04-5 is a valid CAS Registry Number.

81734-04-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-benzylidene-3-oxopentanoate

1.2 Other means of identification

Product number -
Other names (Z)-2-methoxycarbonyl-1-phenyl-1-penten-3-one

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:81734-04-5 SDS

81734-04-5Downstream Products

81734-04-5Relevant academic research and scientific papers

Rhodium carbonyl-catalyzed carbonylation of unsaturated compounds III*. Synthesis of α,β-unsaturated ethyl ketones by cross-hydrocarbonylation of acetylenes and ethylene with carbon monoxide and hydrogen

Hong, Pangbu,Mise, Takaya,Yamazaki, Hiroshi

, p. 129 - 140 (2007/10/02)

Rhodium carbonyl-catalyzed cross-hydrocarbonylation of acetylenes and ethylene with carbon monoxide and hydrogen gives α,β-unsaturated ethyl ketones.Under CO (10 kg cm-2) and H2 (50 kg cm-2) at 90 deg C the reaction of diphenylacetylene with ethylene in the presence of Rh4(CO)12 catalyst gave (E)-1,2-diphenyl-1-penten-3-one (3a) in 91percent yield.Under similar conditions phenylacetylene (1d), 1-hexyne (1e), 3,3-dimethyl-1-butyne (1f), and trimethylsilylacetylene (1g) gave (E)-1-phenyl-1-penten-3-one (3d), (E)-4-nonen-3-one (3e), (E)-6,6-dimethyl-4-hepten-3-one (3f), and (E)-1-trimethylsilyl-1-penten-3-one (3g) in 76, 68, 93, and 62percent respectively.Thus, the reaction of terminal acetylenes proceeds with high stereo- and regioselectivity: the propionyl group is introduced to the less-sterically hindered acetylenic carbon atom.By comparison of the regioselectivity with that in the formation of 5-ethyl-2-(5H)-furanone (2), which is obtained in the presence of a hydrogen donor such as alcohol, these reactions are assumed to include a β-acylvinylrhodium complex as the common key intermediate.

RHODIUM CARBONYL-CATALYZED CROSS-HYDROCARBONYLATION OF ACETYLENES AND ETHYLENE. SYNTHESIS OF α,β-UNSATURATED KETONES

Mise, Takaya,Hong, Pangbu,Yamazaki, Hiroshi

, p. 401 - 404 (2007/10/02)

The cross-hydrocarbonylation of acetylenes and ethylene with CO and H2 in the presence of Rh4(CO)12 gave α,β-unsaturated ethyl ketones regio- and stereoselectively.

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