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Ethyl 2-ethyl-3-hydroxy-butanoate is an organic compound with the chemical formula C8H16O3. It is a colorless liquid with a fruity, ester-like odor. ethyl 2-ethyl-3-hydroxy-butanoate is a derivative of butanoic acid, featuring a hydroxyl group (-OH) at the 3rd carbon and an ethyl group (-CH2CH3) at the 2nd carbon. The ester is formed by the reaction of 2-ethyl-3-hydroxy-butanoic acid with ethanol, resulting in the esterification process. Ethyl 2-ethyl-3-hydroxy-butanoate is commonly used as a flavoring agent in the food and beverage industry, particularly in the production of fruit-flavored products, due to its pleasant aroma reminiscent of fruits like apples and pears. It is also found in natural sources such as fruits, vegetables, and fermented beverages, contributing to their characteristic flavors.

5465-11-2

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5465-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5465-11-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5465-11:
(6*5)+(5*4)+(4*6)+(3*5)+(2*1)+(1*1)=92
92 % 10 = 2
So 5465-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O3/c1-4-7(6(3)9)8(10)11-5-2/h6-7,9H,4-5H2,1-3H3

5465-11-2SDS

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-ethyl-3-hydroxybutanoate

1.2 Other means of identification

Product number -
Other names ethyl 2-ethyl-3-hydroxybutyrate

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:5465-11-2 SDS

5465-11-2Relevant academic research and scientific papers

A facile synthesis of 3,4-disubstituted-1,2-dihydro-5H-pyrrol-2-ones

Bhandari, Kalpana,Sharma

, p. 2467 - 2470 (2007/10/03)

A facile and efficient method for the synthesis of 3,4-disubstituted-1,2- dihydro-5H-pyrrol-2-ones 8a,c-f is reported. The method involves the hydrogenation of cyanohydrins of 2-alkyl-3-oxobutyric acid alkyl esters 1a-f, over Raney Ni at 50 psi to furnish hitherto unknown aminoacetyl intermediates 6a-f in quantitative yields which are cyclised to the targeted compounds.

Chemo-enzymatic alkylation of active methylene compounds

Fuganti,Pedrocchi-Fantoni,Servi

, p. 4195 - 4198 (2007/10/02)

Active methylene compounds undergo chemical condensation in water with aldehydes derived from yeast oxidation of the corresponding alcohols. Unsaturated compounds so obtained are then further reduced by yeast.

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