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2983-05-3

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2983-05-3 Usage

Class

Esters

Common Uses

Flavoring agent in food and beverages, perfumes and cosmetics, pharmaceuticals, and as a solvent in industrial processes

Aroma

Sweet, fruity, and floral

Appearance

Colorless liquid

Molecular Weight

128.18 g/mol

Physical Properties

Soluble in ethanol, propylene glycol, and most oils; slightly soluble in water

Safety Profile

Generally considered safe when used in recommended concentrations, but may cause skin irritation or allergic reactions in some individuals.

Check Digit Verification of cas no

The CAS Registry Mumber 2983-05-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2983-05:
(6*2)+(5*9)+(4*8)+(3*3)+(2*0)+(1*5)=103
103 % 10 = 3
So 2983-05-3 is a valid CAS Registry Number.

2983-05-3SDS

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 3-oxopentan-2-yl acetate

1.2 Other means of identification

Product number -
Other names 2-acetoxypentan-3-one

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:2983-05-3 SDS

2983-05-3Downstream Products

2983-05-3Relevant articles and documents

Chemistry of Dioxiranes. 21. Thermal Reactions of Dioxiranes

Singh, Megh,Murray, Robert W.

, p. 4263 - 4270 (2007/10/02)

Thermolysis of dioxiranes in solutions of their parent ketones or in mixtures of the parent ketone and a foreign ketone leads to the formation of esters.The results are explained by postulating a free-radical mechanism involving H atom abstraction from the ketones.The resulting radicals are converted to the observed esters by reaction with acyloxy radicals derived from homolysis of the dioxiranes.Autodecomposition of dimethyldioxirane in acetone solution at room temperature gives methyl acetate at a very slow rate.When catalyzed by BF3 etherate the same decomposition proceeds much more rapidly and is accompanied by acetol formation.

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