18508-59-3

Basic information

• Product Name: phenyl undec-10-enoate
• Synonyms: phenyl undec-10-enoate;10-Undecenoic acid phenyl ester;Einecs 242-390-7
• CAS NO: 18508-59-3
• Molecular Formula: C₁₇H₂₄O₂
• Molecular Weight: 260.37126
• EINECS: 242-390-7
• Mol File: 18508-59-3.mol

Chemical Properties

• Boiling Point: 366.3°Cat760mmHg
• Flash Point: 123.9°C
• Appearance: /
• Density: 0.961g/cm³
• Vapor Pressure: 1.47E-05mmHg at 25°C
• Refractive Index: 1.495
• CAS DataBase Reference: phenyl undec-10-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl undec-10-enoate(18508-59-3)
• EPA Substance Registry System: phenyl undec-10-enoate(18508-59-3)

Safety Data

• Hazardous Substances Data: 18508-59-3(Hazardous Substances Data)

Usage

Uses

Used in Food and Beverage Industry:
Phenyl undec-10-enoate is used as a flavoring agent to impart a sweet, fruity aroma and taste to food and beverages, enhancing the overall sensory experience for consumers.
Used in Perfume and Cosmetic Industry:
In the perfume and cosmetic industry, phenyl undec-10-enoate is utilized as a fragrance ingredient, adding a pleasant scent to these products and making them more appealing to users.
Used in Soap and Detergent Manufacturing:
Phenyl undec-10-enoate is employed in the production of soaps and detergents, where it serves to improve the fragrance of these cleaning products, making them more attractive to consumers.
Used in Household Product Industry:
This organic compound is also used in the manufacturing of other household products, contributing to the enhancement of their overall fragrance and improving the consumer experience.

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

Upstream product

• 102-09-0 bis(phenyl) carbonate 
• 112-38-9 10-undecenoic acid 
• 538-75-0 dicyclohexyl-carbodiimide 
• 108-95-2 phenol 

Downstream Products

• 5332-51-4 undec-10-enamide 
• 106262-52-6 10-undecenoic acid benzyl ester 
• 7493-76-7 allyl 10-undec-10-enoate 
• 109-42-2 butyl 10-undecenoate 
• 5459-98-3 10-undecenoic acid isopropyl ester 

Relevant articles and documents

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

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).

Selective esterifications of alcohols and phenols through carbodiimide couplings

Esterification of carboxylic acids capable of forming ketene intermediates upon treatment with carbodiimides permits the selective acylation of alcohols in the presence of phenols lacking strong electron-withdrawing groups. The selectivity of acylations involving highly acidic phenols could be reversed through the addition of catalytic amount of acid. Esterification of other carboxylic acids was found to proceed through the formation of symmetric anhydrides and provide the opposite chemoselectivity. In both cases the relative acylation rates of substituted phenols are consistent with a reaction mechanism involving an attack of phenolate anions on electrophilic intermediates such as ketenes and symmetric anhydrides, with the carbodiimides serving both as an activating reagent and as a basic catalyst.