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Usage

Uses

Used in Fragrance Industry:
Norcamphor acetate is used as a key component in the production of fragrances and perfumes due to its pleasant odor. Its high vapor pressure allows for easy release into the air, enhancing the scent and making it a valuable addition to the fragrance industry.
Used in Pharmaceutical and Medicinal Applications:
Norcamphor acetate has been studied for its potential use in pharmaceutical and medicinal applications. Its unique chemical structure and properties make it a promising candidate for further research and development in the medical field.
Used in Research and Development:
Due to its versatile nature and potential for various applications, norcamphor acetate is also utilized in research and development for exploring new uses and understanding its properties better. This includes studying its interactions with other compounds and potential applications in different industries.

Upstream product

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