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3-Penten-2-one, 3-ethyl-, also known as 3-ethyl-3-penten-2-one, is an organic compound with the molecular formula C6H10O. It is a colorless liquid with a strong, pungent odor. This chemical is a member of the enone class, which are unsaturated ketones with a carbon-carbon double bond adjacent to the carbonyl group. 3-Ethyl-3-penten-2-one is used as a flavoring agent and fragrance compound in the food and beverage industry, as well as in the production of various chemicals and pharmaceuticals. It is synthesized through various chemical reactions, such as the aldol condensation of acetone and propionaldehyde, followed by dehydration. Due to its reactive nature, it is important to handle 3-Penten-2-one, 3-ethyl- with care, as it can be harmful if inhaled, ingested, or absorbed through the skin.

1114-37-0

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1114-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1114-37-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1114-37:
(6*1)+(5*1)+(4*1)+(3*4)+(2*3)+(1*7)=40
40 % 10 = 0
So 1114-37-0 is a valid CAS Registry Number.

1114-37-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethylpent-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3-ethyl-pent-3-en-2-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:1114-37-0 SDS

1114-37-0Relevant academic research and scientific papers

FORMATION DE CETONES ETHYLENIQUES PAR ACTION D'ACIDE ACETYLSULFOACETIQUE SUR DES ALCENES

Loiseau, Andre-Michel,Luft, Robert,Zunino, Serge

, p. 144 - 152 (2007/10/02)

Monoalkyl- and 1,2-dialkylethylenes have a similar behaviour under the action of acetylsulfoacetic acid : the reaction does not necessarily stop after the formation of α- or β-enones, the yield of which is highly influenced by reaction time; thus, 1-acetoxy-1,3-dienes are identified in the case of α-enones.A different behaviour is shown by 1,1-dialkyl and trialkylethylenes, which can constitute an interesting source of highly branched enones.With this second group of alkenes, isomerisation of the alkene is sometimes observed prior to acetylation.Lastly, some alkenes undergo acetoxylation at the same time as acetylation.

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