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18508-59-3

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18508-59-3 Usage

General Description

Phenyl undec-10-enoate is an organic compound mainly used as a flavoring agent in food and beverages. It is a colorless to pale yellow liquid with a sweet, fruity odor. Phenyl undec-10-enoate is also used in the production of perfumes and cosmetics due to its pleasant scent. Additionally, it is utilized in the manufacturing of soaps, detergents, and other household products. The compound is synthesized through the esterification of undec-10-enoic acid with phenol, resulting in a chemical that enhances the overall fragrance and taste of various consumer goods. However,

Check Digit Verification of cas no

The CAS Registry Mumber 18508-59-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,0 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18508-59:
(7*1)+(6*8)+(5*5)+(4*0)+(3*8)+(2*5)+(1*9)=123
123 % 10 = 3
So 18508-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H24O2/c1-2-3-4-5-6-7-8-12-15-17(18)19-16-13-10-9-11-14-16/h2,9-11,13-14H,1,3-8,12,15H2

18508-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl undec-10-enoate

1.2 Other means of identification

Product number -
Other names 10-Undecenoic acid,phenyl 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:18508-59-3 SDS

18508-59-3Relevant articles and documents

Base catalyzed sustainable synthesis of phenyl esters from carboxylic acids using diphenyl carbonate

Kreye, Oliver,Meier, Michael A. R.

, p. 53155 - 53160 (2015/06/25)

Phenyl esters were obtained in moderate to high yields by reaction of aliphatic and aromatic carboxylic acids with one equivalent of diphenyl carbonate in the presence of catalytic amounts of tertiary amine bases, such as DBU, TBD and DMAP under neat conditions at elevated temperatures (>100°C).

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