82832-29-9

Basic information

• Product Name: Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-
• Synonyms: Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]- ;4-PENTYL-4'-(4-FLUOROPHENYL)BI(CYCLOHEXANE);1-Fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]benzene;4-(4-Fluorophenyl)-4'-pentyl-1,1'-bi(cyclohexane)
• CAS NO: 82832-29-9
• Molecular Formula: C23H35F
• Molecular Weight: 330.5224032
• Mol File: 82832-29-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-(82832-29-9)
• EPA Substance Registry System: Benzene,1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]-(82832-29-9)

Safety Data

• Hazardous Substances Data: 82832-29-9(Hazardous Substances Data)

Usage

General Description

Benzene, 1-fluoro-4-[(trans,trans)-4'-pentyl[1,1'-bicyclohexyl]-4-yl]- is a complex chemical compound with a molecular structure that includes a benzene ring attached to a fluoro and pentyl group, as well as a bicyclohexyl moiety. It is a fluorinated derivative of 1,1'-bicyclohexyl and may have various industrial applications due to its unique structure. The compound's properties and potential uses would need to be studied further to fully understand its behavior and potential applications.

Upstream product

• 1060659-61-1 trans-4-(trans-4'-pentylcyclohexan-1'-yl)cyclohexan-1-yl p-toluenesulfonate 
• 352-13-6 4-flourophenylmagnesium bromide 
• 149715-70-8 cis-4-bromo-trans-4'-pentyl-1,1'-bi(cyclohexyl) 

Relevant articles and documents

Iron-catalyzed cross-coupling of alkyl sulfonates with arylzinc reagents

Iron-catalyzed cross-coupling reactions of primary and secondary alkyl sulfonates with arylzinc reagents proceed smoothly In the presence of excess TMEDA and a concomitant magnesium salt. The arylzinc reagents are prepared from the corresponding aryllithium or magnesium reagents with ZnI2. The In situ formation of alkyl Iodides and consecutive rapid cross-coupling avoids discrete preparation of the unstable secondary alkyl halides and also achieves high product selectivity.

Reduction of 3-Substituted 1-Arylcyclobutanols

A useful and specific method for the the title reaction (1 → 2) involves treatment with NaBH4 in CF3COOH whereas other procedures from the literature yield hard-to-separate mixtures. 1-Arylcyclohexanols 3 give mainly cyclohexenes with borohydride/trifluoroacetic acid. Their reduction to compounds 4 ,however, is possible with MeSO3H/ NaBH4.