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7460-74-4

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7460-74-4 Usage

Definition

ChEBI: A fatty acid ester obtained by the formal condensation of 2-phenylethanol with valeric acid.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 7460-74-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7460-74:
(6*7)+(5*4)+(4*6)+(3*0)+(2*7)+(1*4)=104
104 % 10 = 4
So 7460-74-4 is a valid CAS Registry Number.

7460-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylethyl pentanoate

1.2 Other means of identification

Product number -
Other names phenethyl pentanoate

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:7460-74-4 SDS

7460-74-4Downstream Products

7460-74-4Relevant articles and documents

Efficient O-Acylation of Alcohols and Phenol Using Cp2TiCl as a Reaction Promoter

Durán-Pe?a, María Jesús,Botubol-Ares, José Manuel,Hanson, James R.,Hernández-Galán, Rosario,Collado, Isidro G.

supporting information, p. 3584 - 3591 (2016/07/28)

A method has been developed for the conversion of primary, secondary, and tertiary alcohols, and phenol, into the corresponding esters at room temperature. The method uses a titanium(III) species generated from a substoichiometric amount of titanocene dichloride together with manganese(0) as a reductant, as well as methylene diiodide. It involves a transesterification from an ethyl ester, or a reaction with an acyl chloride. A radical mechanism is proposed for these transformations.

Solubilizing agents for active or functional organic compounds

-

Page/Page column 3, (2008/06/13)

An active or functional organic compound is solubilized by an ester of an aryl alcohol, e.g., phenethyl, benzyl or substituted benzyl alcohol, and an alkyl or cycloalkyl carboxylic acid, or by a carbonate of said aryl alcohol and an alkyl or cycloalkyl carbonic acid.

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