13038-22-7

Basic information

• Product Name: ACETIC ACID 8-NONEN-1-YL ESTER
• Synonyms: 8-NONENYL ACETATE;8-NONEN-1-YL ACETATE;9-ACETOXY-1-NONENE;ACETIC ACID 8-NONEN-1-YL ESTER;Acetic Acid 8-Nonenyl Ester;8-Nonene-1-ol acetate;9-Acetoxy-1-nonene Acetic Acid 8-Nonenyl Ester
• CAS NO: 13038-22-7
• Molecular Formula: C₁₁H₂₀O₂
• Molecular Weight: 184.28
• Mol File: 13038-22-7.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 155 °C / 24mmHg
• Appearance: /
• Density: 0.88
• Refractive Index: 1.4330-1.4350
• CAS DataBase Reference: ACETIC ACID 8-NONEN-1-YL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: ACETIC ACID 8-NONEN-1-YL ESTER(13038-22-7)
• EPA Substance Registry System: ACETIC ACID 8-NONEN-1-YL ESTER(13038-22-7)

Safety Data

• Hazardous Substances Data: 13038-22-7(Hazardous Substances Data)

Usage

General Description

ACETIC ACID 8-NONEN-1-YL ESTER is a chemical compound consisting of acetic acid and 8-nonen-1-yl ester. It is commonly used as a flavoring agent in the food and beverage industry, providing a fruity and floral aroma to various products. This chemical also has applications in the fragrance and cosmetics industries, where it is incorporated into perfumes, colognes, and personal care products. Additionally, ACETIC ACID 8-NONEN-1-YL ESTER is used in the production of soaps, detergents, and other household products due to its pleasant scent and ability to mask odors. Overall, this chemical compound serves as a versatile ingredient with a wide range of applications in various industries.

InChI:InChI=1/C11H20O2/c1-3-4-5-6-7-8-9-10-13-11(2)12/h3H,1,4-10H2,2H3

Upstream product

• 13038-21-6 non-8-en-1-ol 
• 75-36-5 acetyl chloride 
• 108-24-7 acetic anhydride 
• 7433-78-5 cis-5-decene 
• 201230-82-2 carbon monoxide 
• 64-19-7 acetic acid 
• 3710-30-3 1,7-Octadiene 
• 13175-44-5 oct-7-en-1-ol 
• 5048-34-0 non-8-enenitrile 
• 39770-04-2 8-nonen-1-al 
• 2695-47-8 6-Bromo-1-hexene 
• 31642-67-8 non-8-enoic acid 
• 3937-56-2 1,9-Nonanediol 
• 92038-37-4 10-acetoxydecanoic acid 

Downstream Products

• 1730-95-6 (3S,6S)-3,6-dimethyloctane 
• 74630-25-4 8-methyl-2-decene 
• 1160106-03-5 C₁₈H₃₆ 
• 1160106-04-6 (S,E)-14-methyl-8-hexadecenyl acetate 
• 1428904-12-4 Z-hexa-8-decen-dinyl 1,16-diacetate 
• 1160105-93-0 C₂₀H₃₆O₄ 
• 19689-19-1 5-decene 
• 64437-30-5 (Z)-tridec-8-en-1-yl acetate 
• 33956-49-9 (8E,10E)-dodeca-8,10-dienol 
• 53880-51-6 (E,E)-8,10-dodecadienyl acetate 
• 28079-04-1 (Z)-8-dodecen-1-yl acetate 

Relevant articles and documents

Novel convenient synthesis of (Z/E)-8-dodecenyl acetates, components of the Grapholitha molesta sex pheromone

Components of the Grapholitha molesta sex pheromone, (Z/E)-8-dodecenyl acetates (1, 2), were synthesized in five steps in 20% overall yield using 10-hydroxydecanoic acid (3) as starting material.

Ruthenium-catalysed domino hydroformylation-hydrogenation-esterification of olefins

A novel catalytic domino reductive hydroformylation-esterification of olefins is reported. The optimal protocol makes use of an inexpensive Ru carbonyl catalyst and uses acetic acid as both solvent and reactant. In general, moderate to good yields are obtained using aliphatic or aromatic olefins including industrially relevant di-isobutene. This atom-efficient catalytic transformation provides straightforward access to various acetate esters from unfunctionalized olefins.

SYNTHESIS OF PHEROMONES AND RELATED MATERIALS VIA OLEFIN METATHESIS

Methods for preparation of olefins, including 8- and 11-unsaturated monoenes and polyenes, via transition metathesis-based synthetic routes are described. Metathesis reactions in the methods are catalyzed by transition metal catalysts including tungsten-, molybdenum-, and ruthenium-based catalysts. The olefins include insect pheromones useful in a number of agricultural applications.

PALLADIUM-CATALYZED DECARBONYLATION OF FATTY ACID ANHYDRIDES FOR THE PRODUCTION OF LINEAR ALPHA OLEFINS

The present invention is directed to methods of forming olefins, especially linear alpha olefins from fatty acids or anhydrides, each method comprising: contacting an amount of precursor carboxylic acid anhydride with a palladium catalyst comprising a bidentate bis-phosphine ligand in a reaction mixture so as to form an olefin in a product with the concomittant formation and removal of CO and water from the reaction mixture, either directly or indirectly, wherein the reaction mixture is maintained with a sub-stoichiometric excess of a sacrificial carboxylic acid anhydride, an organic acid, or both, said sub-stoichiometric excess being relative to the amount of the precursor carboxylic acid anhydride. The precursor carboxylic acid anhydride may be added to the reaction mixture directly or formed in situ by the reaction between at least one precursor carboxylic acid with a stoichiometric amount of the sacrificial acid anhydride.