790-30-7

Basic information

• Product Name: 1,1'-Biphenyl, 4-(cyclohexylmethyl)-
• CAS NO: 790-30-7
• Molecular Formula: C19H22
• Molecular Weight: 250.384
• Mol File: 790-30-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,1'-Biphenyl, 4-(cyclohexylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-Biphenyl, 4-(cyclohexylmethyl)-(790-30-7)
• EPA Substance Registry System: 1,1'-Biphenyl, 4-(cyclohexylmethyl)-(790-30-7)

Safety Data

• Hazardous Substances Data: 790-30-7(Hazardous Substances Data)

Usage

Structure

A derivative of biphenyl with a cyclohexylmethyl group attached to the fourth position of one of the benzene rings.

Usage

Building block in the synthesis of various organic compounds.

Applications

Pharmaceutical, agrochemical, and material industries.

Biological and pharmacological properties

Studied for potential anti-inflammatory and anti-cancer activities.

Versatility

Range of potential applications in different industries.

Upstream product

• 613-42-3 4-benzylbiphenyl 
• 110-82-7 cyclohexane 
• 84648-91-9 biphenyl-4-yldiazomethane 
• 2128-93-0 biphenyl-4-yl-phenyl-methanone 
• 2051-62-9 4'-biphenyl chloride 
• 108-85-0 1-bromocyclohexane 
• 91954-74-4 4-phenylbenzylidene hydrazine 
• 3218-36-8 4-Phenylbenzaldehyde 
• 626-62-0 Cyclohexyl iodide 

Relevant articles and documents

Site-Selective C–H Benzylation of Alkanes with N-Triftosylhydrazones Leading to Alkyl Aromatics

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Nickel-Catalyzed Cross-Coupling of Umpolung Carbonyls and Alkyl Halides

An effective nickel-catalyzed cross-coupling of Umpolung carbonyls and alkyl halides was developed. Complementary to classical alkylation techniques, this reaction utilizes Umpolung carbonyls as the environmentally benign alkyl nucleophiles, providing an efficient and selective catalytic alternative to the traditional use of highly reactive alkyl organometallic reagents.

Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides-reaction discovery using parallel microscale experimentation

Microscale parallel experimentation was used to discover three catalyst systems capable of coupling secondary organotrifluoroborates with sterically and electronically demanding aryl chlorides and bromides. The ensuing results represent the first comprehensive study of alkylboron coupling to aryl chlorides and, in particular, using secondary alkylboron partners. A ligand-dependent β-hydride elimination/reinsertion mechanism was implicated in the cross-coupling of more hindered substrates, leading to isomeric mixtures of coupled products in some cases. Copyright