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2408-20-0

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2408-20-0 Usage

Chemical Properties

A colorless liquid with sharp, sour, fruity odor and ethereal fruity (apricot, apple) taste

Preparation

By direct esterification of the acid with allyl alcohol in benzene solution in the presence of concentrated H2SO4, or of p-toluene sulfonic acid.

Taste threshold values

Taste characteristics at 10 ppm: pungent, sharp, alliaceous, acrylate-like with a tropical depth.

Flammability and Explosibility

Flammable

Check Digit Verification of cas no

The CAS Registry Mumber 2408-20-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2408-20:
(6*2)+(5*4)+(4*0)+(3*8)+(2*2)+(1*0)=60
60 % 10 = 0
So 2408-20-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2/c1-3-5-8-6(7)4-2/h3H,1,4-5H2,2H3

2408-20-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name prop-2-enyl propanoate

1.2 Other means of identification

Product number -
Other names FEMA No. 2040

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:2408-20-0 SDS

2408-20-0Relevant articles and documents

Cyclization of allyl α-halocarboxylates in the presence of metallocomplex initiators

Terent'ev,Vasil'eva,Kuz'mina,Mysov,Belokon

, p. 764 - 766 (1997)

Allyl trichloroacetate and allyl 2,2-dichloropropionate, unlike allyl bromoacetate and allyl 2-bromopropionate, undergo cyclization into γ-lactones in the presence of a Fe(CO)5-amide system. All these esters undergo reductive dehalogenation under the action of the Bun3SnH-AlBN system.

Method for preparing propionate by ester alcohol exchange

-

Paragraph 0038-0039, (2019/07/04)

The invention discloses a method for preparing propionate by ester alcohol exchange, and relates to a method for preparing propionate. According to the invention, the method for synthesizing propionate by ester alcohol exchange of methyl propionate and various alcohols (including monohydric alcohols such as ethanol, propanol, butanol, tert-butanol, isopropanol, cyclohexanol, allyl alcohol and thelike, dihydric alcohols such as 1,3-propylene glycol and the like, glycerol and the like) is adopted, and methyl propionate and the alcohols are used as raw materials to carry out a reaction under catalysis of alkaline ionic liquid, soluble strong alkali or solid alkali to prepare higher propionate and methanol. According to the method, the synthetic route is short, and the reaction product is taken out through azeotropic extraction of the methyl propionate and methanol, so that the reaction is more thorough, and the target product is directly obtained by one step. The product obtained by thereaction only contains propionate and methanol, the whole reaction process is concise and efficient and is free of pollution, no byproducts are generated, and great significance is achieved for large-scale and low-cost production of propionate.

Synthesis of unsaturated esters via highly efficient esterification catalyzed by polymer grafted quarternary ammonium salts as triphase catalysts

Liang, Zheng Yong,Wang, Li Li,Liu, Hui,Huang, Jin Shuo

, p. 1558 - 1561 (2013/09/12)

A series of unsaturated esters were prepared via condensation of sodium carboxylates and alkenyl halide under the condition of macroporous polystyrene grafted quarternary ammonium salt as recyclable phase transfer catalyst, NaI as co-catalyst, Cu powder as inhibitor and H2O as solvent. Under optimal conditions, products yields are 78.2~ 96.0%. The catalyst can be convenient recycled and reutilized for about five times without losing its activity obviously.

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