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1-phenylprop-1-en-2-yl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5351-09-7

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5351-09-7 Usage

Physical state

Colorless to pale yellow liquid

Usage

Production of perfumes, flavoring agent in food products

Functionality

Ester (formed by the reaction between an alcohol and an acid)

Odor

Sweet, floral

Common use

Adding warm, sweet, and floral notes to perfumes and scented products

Benefits

Antimicrobial and antioxidant properties

Industries

Food, cosmetic

Precaution

Can cause skin and eye irritation (should be handled with care)

Check Digit Verification of cas no

The CAS Registry Mumber 5351-09-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5351-09:
(6*5)+(5*3)+(4*5)+(3*1)+(2*0)+(1*9)=77
77 % 10 = 7
So 5351-09-7 is a valid CAS Registry Number.

5351-09-7SDS

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 1-PHENYL-1-PROPEN-2-OL BENZOATE

1.2 Other means of identification

Product number -
Other names BENZOIC ACID,1-CYCLOHEXYL-2-PROPYN-1-YL ESTER

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:5351-09-7 SDS

5351-09-7Relevant academic research and scientific papers

Ruthenium-Catalyzed Hydrocarboxylation of Internal Alkynes

Jeschke, Janine,Engelhardt, Tony B.,Lang, Heinrich

, p. 1548 - 1554 (2016/04/05)

The application of the highly efficient ruthenium catalyst [Ru(CO)2{P(p-CF3-C6H4)3}2(O2CPh)2] (1) in the selective syn-addition of carboxylic acids to internal alkynes

Trifluoromethanesulfonic acid catalyzed isomerization of kinetic enol derivatives to the thermodynamically favored isomers

Lee, Phil Ho,Kang, Dongjin,Choi, Subin,Kim, Sunggak

, p. 3470 - 3473 (2011/08/22)

Trifluoromethanesulfonic acid catalyzed isomerization of kinetic enol derivatives to the thermodynamically favored isomers was developed. Under the present conditions, kinetic enol phosphates, enol acetates and benzoates, and enol sulfonates were smoothly isomerized to produce the corresponding thermodynamically favored isomers in good to excellent yields.

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