3716-38-9

Usage

Uses

Used in Perfumery and Personal Care Industry:
2,3,3a,4,5,6,7,7a-octahydro-1H-inden-5-ol is used as a fragrance ingredient for its pleasant, floral-like scent, enhancing the aroma of perfumes and personal care products.
Used in Food Industry:
As a flavoring agent, 2,3,3a,4,5,6,7,7a-octahydro-1H-inden-5-ol is employed to impart a specific taste or aroma to food products, contributing to the overall sensory experience of the consumer.
Used in Pharmaceutical Industry:
2,3,3a,4,5,6,7,7a-octahydro-1H-inden-5-ol has potential applications in the pharmaceutical industry, where it may be utilized in the development of new drugs or as an intermediate in the synthesis of existing medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3,3a,4,5,6,7,7a-octahydro-1H-inden-5-ol may be used as a component in the formulation of pesticides, herbicides, or other agricultural chemicals, potentially contributing to the effectiveness of these products.

InChI:InChI=1/C9H16O/c10-9-5-4-7-2-1-3-8(7)6-9/h7-10H,1-6H2

Upstream product

• 1470-94-6 5-hydroxy-2,3-dihydro-1H-indene 
• 90642-40-3 bicyclo<4.3.0>nona-2,9-diene 
• 3048-65-5 cis-bicyclo<4.3.0>nona-3,7-diene 
• 56170-01-5 cis-bicyclo<4.3.0>nona-2,7-diene 
• 74459-91-9 (1R,7aS)-2,3,3a,4,7,7a-Hexahydro-1H-inden-1-ol 
• 36237-87-3 trans-8-hydroxybicyclo<4.3.0>-3-nonene 
• 3048-65-5 trans bicyclo<4.3.0>nona-3,7-diene 
• 7603-35-2 (3aS,7aR)-3a,6,7,7a-Tetrahydro-1H-indene 
• 119594-91-1 (+/-)-cis-bicyclo<4.3.0>nonane-3,8-dione 
• 119594-92-2 (+/-)-trans-bicyclo<4.3.0>nonan-3-one 
• 60844-61-3 trans-bicyclo<4.3.0>non-3-ene 
• 7077-14-7 (+/-)-(3arH,7atH)-Hexahydro-indan-carbonsaeure-(5t) 
• 119595-00-5 (+/-)-(trans-cyclohex-4-ene-1,2-diyl)-di-acetonitrile 
• 119595-01-6 trans-4,5-bis(carboxymethyl)cyclohexene 

Downstream Products

• 4668-91-1 (+/-)-cis-bicyclo<4.3.0>nonan-3-one 
• 5686-84-0 octahydro-5H-inden-5-one 

Relevant academic research and scientific papers

Enzymes in Organic Synthesis. 46. Regiospecific and Stereoselective Horse Liver Alcohol Dehydrogenase Catalyzed Reductions of cis- and trans-Bicyclononanones

Further evidence for the preference of horse liver alcohol dehydrogenase for six-membered rather than five-membered ring ketone substrates is presented.This chemospecificity can be exploited preparatively, as illustrated by the HLADH-catalyzed reductions

HYDROBORATION AND OXYMERCURATION-DEMERCURATION OF CIS-BICYCLONONA-3,7-DIENE. SYNTHESIS OF CIS-BICYCLONONENONES

Four isomeric cis-bicyclononenones were obtained from cis-bicyclonona-3,7-diene by hydroboration and oxymercuration-demercuration.Their structures were determined by means of their 13C NMR spectra.The addition of the hydroborating agents takes place preferentially (60-80percent) at the cyclopentene double bond at the C7 and C8 atoms and is most selective in the case of 9-borabicyclononane.The direction of addition of mercuric acetate depends on the solvent; the reaction takes place most selectively (95percent) at the cyclohexene double bond in 1:9 aqueous THF, and here the mercury adds to the C4 carbon atom to the extent of 90percent.

A REGIOSPECIFIC DOUBLE BOND SHIF INDUCED BY TITANOCENE CATALYSTS

cis-Bicyclo(4.3.0)-3,7-nonadien is isomerized by titanocene-derived catalysts to bicyclo(4.3.0)-2,9-nonadiene.