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2,4-Decadienoic acid, ethyl ester, (2Z,4E)- is an organic compound with the chemical formula C12H20O2. It is a positional isomer of other deca-2,4-dienoic acid esters, characterized by the presence of two carbon-carbon double bonds in the 2 and 4 positions. The molecule consists of a deca-2,4-dienoic acid moiety, which is esterified with an ethyl group. 2,4-Decadienoic acid, ethyl ester, (2Z,4E)- is known for its unique chemical properties and potential applications in various fields, such as the synthesis of fragrances, flavorings, and pharmaceuticals. It is also used as a chemical intermediate in the production of various specialty chemicals. The (2Z,4E)- configuration indicates the specific arrangement of the double bonds, which influences the compound's reactivity and physical properties.

3025-31-8

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3025-31-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3025-31-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3025-31:
(6*3)+(5*0)+(4*2)+(3*5)+(2*3)+(1*1)=48
48 % 10 = 8
So 3025-31-8 is a valid CAS Registry Number.

3025-31-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,4-decadienoate

1.2 Other means of identification

Product number -
Other names -

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:3025-31-8 SDS

3025-31-8Relevant academic research and scientific papers

Synthesis of all four isomers of (E)-4,5-dihydroxydec-2-enal using osmium-catalysed asymmetric dihydroxylation

Allevi, Pietro,Tarocco, Giorgio,Longo, Alessandra,Anastasia, Mario,Cajone, Francesco

, p. 1315 - 1325 (2007/10/03)

The enantioselective synthesis of the four possible isomers of (E)-4,5-dihydroxydec-2-enal, a cytotoxic product formed in peroxidised liver microsomal lipids, is accomplished via a Sharpless AD reaction alone or associated as appropriate with a regioselective epimerisation of one of the introduced hydroxy groups.

Conversion of 2-Sulfinylated 2-Alkenoate Esters to (2E,4E)-2,4-Alkadienoate Esters by Pyrolysis

Tanikaga, Rikuhei,Nozaki, Yoshihito,Nishida, Masaharu,Kaji, Aritsune

, p. 729 - 733 (2007/10/02)

Thermal reaction of ethyl (2E)-2-phenylsulfinyl-2-alkenoates (E-2) prepared from aldehydes and ethyl 2-phenylsulfinylacetate have been investigated.Refluxing of E-2 or their Z-isomers in xylene resulted in the formation of ethyl (2E,4E)-2,4-alkanedioates accompanied by ethyl (2E)-4-hydroxy-2-alkenoates.Ethyl 2-cycloalkylidene-2-phenylsulfinylacetates were found to be more susceptible to pyrolysis.The enoate esters (2) undergo migration of their carbon-carbon double bond and then sigmatropic rearrangement to benzenesulfenate esters, followed by thermolytic extrusion of a benzenesulfenic acid probably via ethyl(2E)-4-phenylsulfinyl-2-alkenoates to afford ethyl (2E,4E)-2,4-alkadienoates.

A Novel Stereoselective Synthesis of the "Pear Ester" Ethyl (2E,4Z)-2,4-Decadienoate

Bestmann, Hans Juergen,Suess, Joachim

, p. 363 - 365 (2007/10/02)

The title compound 8 is prepared by two stereoselective Wittig olefinations.

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