4057-31-2

Usage

Uses

Used in Flavor and Fragrance Industry:
(1,3,3-trimethylnorbornan-2-yl) acetate is used as a flavoring agent and fragrance ingredient for its pleasant, fruity odor. It is commonly incorporated into perfumes, colognes, and other scented products to enhance their aroma and appeal to consumers.
Used in Pharmaceutical Industry:
Due to its unique chemical structure and properties, (1,3,3-trimethylnorbornan-2-yl) acetate has potential applications in the pharmaceutical industry. It may be utilized in the development of new drugs or as an intermediate in the synthesis of pharmaceutical compounds.
Used in Agrochemical Industry:
(1,3,3-trimethylnorbornan-2-yl) acetate also has potential applications in the agrochemical industry. It may be used in the development of new agrochemical products or as an intermediate in the synthesis of agrochemical compounds, contributing to advancements in agriculture and pest control.

Upstream product

• 36386-49-9 fenchol 
• 64-19-7 acetic acid 
• 5813-49-0 nitrosyl acetate 
• 13293-47-5 2αH-pinan-3α-ylamine 

Relevant academic research and scientific papers

1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol in Nucleophilic Substitution Reactions

1,3,3-Trimethylbicyclo[2.2.1]heptan-2-endo-ol (fenchol) reacts with acetonitrile in the presence of sulfuric acid to selectively form an isofenchane derivative - N-acetyl-1,5,5-trimethylbicyclo[2.2.1]heptan-2-exo-amine as a result of nucleophilic addition at the most accessible carbon atom of a nonclassical 1,3,3-trimethylbicyclo[2.2.1]heptyl cation. The H2SO4-catalyzed reaction with acetic acid results in exclusive formation of 1,3,3-trimethylbicyclo[2.2.1]hept-2-exo-yl acetate, implying an SN2 reaction mechanism.

Rearrangement of Pinane Derivatives. Part 8. Deamination of 2αH-Pinan-3α-ylamine

Solvolysis of 2αH-pinan-3α-yl toluene-p-sulphonate has been shown to proceed with concomitant 1,2-hydride shift to give the pinan-2-yl carbocation.Contrary to earlier reports, this species reacts normally to give, in good yield, pinan-2-yl substitution products.In contrast the pinan-3-ylamines react via a similar route, but give much smaller amounts of pinan-2-yl products.The usual reasons for differences between solvolysis and deamination (i.e. the intermediacy of diazonium ions and/or high-energy ions) can be discounted, and possible reasons for the differences in behaviour are discussed.