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2396-83-0

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2396-83-0 Usage

Chemical Properties

Ethyl 3-hexenoate has a green, fruity aroma.

Occurrence

Reported found in pineapple, melon, beer, passion fruit juice, quince, plumcot, prickly pear and kiwifruit.

Definition

ChEBI: A fatty acid ethyl ester of 3-hexenoic acid.

Preparation

From3-hexenoic acid and dicyclohexylcarbodimide; by fungalfermentation (20°C) of 3-hexenoic acid using Saccharomyces cerevisiae; from trialkylboranes and ethyl-4-bromocrotonate in the presence of 2,6-di-tert-butyl-phenoxide; by pyrolysis of acetates.

Taste threshold values

Taste characteristics at 10 ppm: fruity, green, sweet and pineapple-like.

General Description

Ethyl trans-3-hexenoate is an ester. It was evaluated as aroma volatile in the GC effluents of cashew apple water phase phase.

Check Digit Verification of cas no

The CAS Registry Mumber 2396-83-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2396-83:
(6*2)+(5*3)+(4*9)+(3*6)+(2*8)+(1*3)=100
100 % 10 = 0
So 2396-83-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h5-6H,3-4,7H2,1-2H3/b6-5+

2396-83-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Packaging
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  • Detail
  • Alfa Aesar

  • (A19734)  Ethyl 3-hexenoate, 98%   

  • 2396-83-0

  • 5g

  • 373.0CNY

  • Detail
  • Alfa Aesar

  • (A19734)  Ethyl 3-hexenoate, 98%   

  • 2396-83-0

  • 25g

  • 748.0CNY

  • Detail

2396-83-0SDS

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 ethyl 3-hexenoate

1.2 Other means of identification

Product number -
Other names trans-ethyl hex-3-enoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:2396-83-0 SDS

2396-83-0Relevant articles and documents

Synthesis of α,β- and β-Unsaturated Acids and Hydroxy Acids by Tandem Oxidation, Epoxidation, and Hydrolysis/Hydrogenation of Bioethanol Derivatives

Faria, Jimmy,Komarneni, Mallik R.,Li, Gengnan,Pham, Tu,Resasco, Daniel E.,Ruiz, Maria P.,Santhanaraj, Daniel

supporting information, p. 7456 - 7460 (2020/03/23)

We report a reaction platform for the synthesis of three different high-value specialty chemical building blocks starting from bio-ethanol, which might have an important impact in the implementation of biorefineries. First, oxidative dehydrogenation of ethanol to acetaldehyde generates an aldehyde-containing stream active for the production of C4 aldehydes via base-catalyzed aldol-condensation. Then, the resulting C4 adduct is selectively converted into crotonic acid via catalytic aerobic oxidation (62 % yield). Using a sequential epoxidation and hydrogenation of crotonic acid leads to 29 % yield of β-hydroxy acid (3-hydroxybutanoic acid). By controlling the pH of the reaction media, it is possible to hydrolyze the oxirane moiety leading to 21 % yield of α,β-dihydroxy acid (2,3-dihydroxybutanoic acid). Crotonic acid, 3-hydroxybutanoic acid, and 2,3-dihydroxybutanoic acid are archetypal specialty chemicals used in the synthesis of polyvinyl-co-unsaturated acids resins, pharmaceutics, and bio-degradable/ -compatible polymers, respectively.

"Syn-Effect" in the Conversion of (E)-α,β-Unsaturated Esters to the Corresponding β,γ-Unsaturated Esters

Guha, Samar Kumar,Shibayama, Atsushi,Abe, Daisuke,Ukaji, Yutaka,Inomata, Katsuhiko

, p. 778 - 779 (2007/10/03)

The stereochemistry in the conversion of (E)-α,β-unsaturated esters to the corresponding β,γ-unsaturated esters by treatment with lithium hexamethyldisilazide in the presence of HMPA was investigated. The Z/E ratios of the resulting β,γ-unsaturated esters varied according to the γ-substituents of the (E)-α,β-unsaturated esters. This phenomenon was rationalized by "syn-effect" which may be attributed primarily to σ → π* interaction and/or 6π-electron homoaromaticity.

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