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932-85-4

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932-85-4 Usage

General Description

5-Ethoxy-4,5-dihydro-2(3H)-furanone is a chemical compound with the molecular formula C6H10O3. It is also known as ethyl 2-oxo-4,5-dihydrofuran-5-ylacetate. 5-Ethoxy-4,5-dihydro-2(3H)-furanone is commonly used in the flavor and fragrance industry, where it is often used in the production of food additives and perfumes. It has a fruity, pineapple-like odor, and is often used to impart a sweet, caramelized note to various products. Additionally, it has been studied for its potential antimicrobial and insecticidal properties. However, it is important to note that this compound may have harmful effects if ingested or inhaled and should be handled with care.

Check Digit Verification of cas no

The CAS Registry Mumber 932-85-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 932-85:
(5*9)+(4*3)+(3*2)+(2*8)+(1*5)=84
84 % 10 = 4
So 932-85-4 is a valid CAS Registry Number.

932-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethoxyoxolan-2-one

1.2 Other means of identification

Product number -
Other names 5-Aethoxy-dihydro-furan-2-on

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:932-85-4 SDS

932-85-4Downstream Products

932-85-4Relevant articles and documents

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Fife

, p. 271 (1965)

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The complete stereochemistry of the enzymatic dehydration of 4-hydroxybutyryl coenzyme A to crotonyl coenzyme A

Friedrich, Peter,Darley, Daniel J.,Golding, Bernard T.,Buckel, Wolfgang

, p. 3254 - 3257 (2008/12/23)

(Chemical Equation Presented) The stereospecific action of the microbial enzyme 4-hydroxybutyryl-CoA dehydratase on the three prochiral centers of its substrate 4-hydroxybutyryl-CoA can now be described as anti elimination of the 2Re and 3Si hydrogen atoms with retention of configuration during the substitution of the hydroxy group by a hydrogen atom. The results confirm the relationship of the dehydratase to acyl-CoA dehydrogenases and the view that the Fe4S4 cluster acts as a Lewis acid.

THE TRANSFORMATION OF ALKENES INTO γ-LACTONES USING α-IODOESTERS

Kraus, George A.,Landgrebe, Kevin

, p. 3939 - 3942 (2007/10/02)

Iodostannyl esters react with alkenes in the presence of AIBN to afford γ-lactones.

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