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2-Ethyl-2-hexenoic acid, 95%, predominantly trans, is a chemical compound with the molecular formula C8H14O2. It is an organic acid that belongs to the class of aliphatic carboxylic acids. 2-ETHYL-2-HEXENOIC ACID, 95%, PREDOMINAN TLY TRANS is characterized by a hexenoic acid chain with an ethyl group attached to the second carbon atom. The 95% purity indicates that the product contains a minimum of 95% of the desired compound, with the remaining 5% being other substances. The predominantly trans descriptor refers to the geometric isomerism of the double bond in the molecule, where the trans configuration is the major form present. This chemical is used in various applications, such as in the synthesis of fragrances and pharmaceuticals, due to its unique properties and reactivity.

5309-52-4

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5309-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5309-52-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5309-52:
(6*5)+(5*3)+(4*0)+(3*9)+(2*5)+(1*2)=84
84 % 10 = 4
So 5309-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H23N3O5S/c1-2-25-17(22)14-11-4-3-5-12(19-23)15(11)26-16(14)18-13(21)10-20-6-8-24-9-7-20/h19,23H,2-10H2,1H3/b18-16-

5309-52-4SDS

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-ethylhex-2-enoic acid

1.2 Other means of identification

Product number -
Other names 2-HEXENOIC ACID,2-ETHYL-

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:5309-52-4 SDS

5309-52-4Downstream Products

5309-52-4Relevant academic research and scientific papers

Transfer-hydrogenation process

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Page/Page column 15; 16, (2018/06/19)

A transfer-hydrogenation process for preparing a carbonyl compound and an alcohol compound comprises the steps of (a) contacting a first carbonyl compound with a first alcohol compound in the presence of a transfer-hydrogenation catalyst in a first reaction zone at conditions effective to form a second carbonyl compound from the first alcohol compound and a second alcohol compound from the first carbonyl compound, and (b) removing the second carbonyl compound from the first reaction zone during step (a). The first carbonyl compound is a saturated aldehyde or ketone, or an α,β-unsaturated aldehyde or ketone. The first alcohol compound is a primary or secondary alcohol. The second alcohol compound is α,β-saturated. The transfer-hydrogenation catalyst includes a Group 8 to 11 metal. This process is useful for preparing and higher value alcohols, such as butanol or 2-ethylhexanol, from the corresponding carbonyl compounds by engaging lower alcohol (C2-C4) feedstocks instead of hydrogen (H2).

OXIDATION OF UNSATURATED ALDEHYDES BY PEROXY ACIDS

Pikh, Z. G.,Samarik, V. Ya.

, p. 1294 - 1306 (2007/10/02)

The full composition of the products and the kinetics of their accumulation was studied during the oxidation of a series of unsaturated aldehydes by peroxy acids.The effects of the temperature, the structure of the aldehyde, and the solvent on the reaction rate and quantitative composition of the products were determined.A kinetic model of the reaction is proposed, and its parameters are calculated.New data are obtained on the mechanism of the Baeyer-Villiger reaction as applied to the oxidation of unsaturated aldehydes by peroxy acids.

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