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Usage

Uses

Used in Perfume and Fragrance Industry:
[1S-(1alpha,2alpha,3beta,5alpha)]-3,6,6-trimethylbicyclo[3.1.1]hept-3-yl acetate is used as a key ingredient in the production of perfumes and fragrances for its pleasant scent, contributing to the creation of various olfactory compositions.
Used in Pharmaceutical Industry:
[1S-(1alpha,2alpha,3beta,5alpha)]-3,6,6-trimethylbicyclo[3.1.1]hept-3-yl acetate may be used as a building block or intermediate in the synthesis of pharmaceutical compounds, leveraging its unique chemical structure for the development of new drugs.
Used in Flavor Industry:
[1S-(1alpha,2alpha,3beta,5alpha)]-3,6,6-trimethylbicyclo[3.1.1]hept-3-yl acetate could be utilized as a component in the flavor industry, where its distinct odor can be employed to enhance or create novel taste profiles in the food and beverage sector.

Upstream product

• 33045-02-2 trans-pinocarvyl acetate 
• 1196-00-5 (+)-isopinocampheol 
• 108-24-7 acetic anhydride 
• 110-82-7 cyclohexane 
• 18172-67-3 beta-pinene 
• 19894-98-5 6,6-dimethyl-2-methylene-bicyclo[3.1.1]heptan-3-ol 
• 2734-31-8 (1R,2R,3S,5S)-(+)-neoisopinocampheol 
• 19889-99-7 (+)-(Z)-pinocarveol 
• 24041-60-9 (+)-isopinocampheol 
• 18492-59-6 (+)-pinocamphone 
• 19889-94-2 (1R)-(2endoH)-pinan-3endo-ol 
• 473-62-1 (1R,2R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptan-3-one 
• 1196-00-5 (-)-isopinocampheol 
• 1674-08-4 (-)-trans-pinocarveol 

Relevant academic research and scientific papers

Chemically synthesized and cross-linked PDMS as versatile alignment medium for organic compounds

A useful procedure for the preparation of chemically synthesized and cross-linked polydimethylsiloxane (PDMS) gels is presented, which does not require β-irradiation for cross-linking. NMR spectra of high quality are obtained, such that even mixtures of compounds exhibiting similar NMR spectra like interconverting stereoisomers can be investigated in the residual dipolar coupling (RDC) approach of organic structure determination.

ENANTIOSELECTIVITY IN THE HYDROLYSIS OF BICYCLIC MONOTERPENE ACETATES WITH THE CULTURED CELLS OF NICOTIANA TABACUM

Key Word Index - Nicotiana tabacum; Solanaceae; tissue culture; biotransformation; hydrolysis; enantioselectivity; bicyclic monoterpene acetates.The enantioselectivity in the hydrolysis of bornyl acetate; isobornyl acetate and isopinocampheyl acetate with the cultured cells of Nicotiana tabacum was investigated.The cultured cells were found to have the ability to hydrolyse enantioselectively the acetates, of which the configuration at the carbon atom bearing the acetoxyl group is R.