159389-47-6

Basic information

• Product Name: 2-bromo-1-cyclohexene-1-carbonyl chloride
• Synonyms: 2-bromo-1-cyclohexene-1-carbonyl chloride
• CAS NO: 159389-47-6
• Molecular Weight: 223.497
• Mol File: 159389-47-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-bromo-1-cyclohexene-1-carbonyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-1-cyclohexene-1-carbonyl chloride(159389-47-6)
• EPA Substance Registry System: 2-bromo-1-cyclohexene-1-carbonyl chloride(159389-47-6)

Safety Data

• Hazardous Substances Data: 159389-47-6(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 38127-47-8 2-bromocyclohex-1-ene-1-carbaldehyde 
• 68965-62-8 2-bromocyclohex-1-enecarboxylic acid 

Downstream Products

• 552857-10-0 2-bromo-N-phenyl-1-cyclohexene-1-carboxamide 

Relevant articles and documents

Access to Cyclopropyl-Fused Azacycles via a Palladium-Catalyzed Direct Alkenylation Strategy

Palladium-catalyzed direct alkenylation of cyclopropyl C-H bonds proceeds in high efficiency. This transformation provides access to novel cyclopropyl-fused azacycles. Ligand studies suggest that bisphosphine monoxide analogues of dppf and rac-BINAP are t

A general strategy for visible-light decaging based on the quinone: Cis -alkenyl lock

Combining the fast thermal cyclization of o-coumaric acid derivatives with the intramolecular photoreduction of quinones gives new visible-light photoremovable protecting groups absorbing well above 450 nm.

CuI/amino acid-catalyzed coupling and cyclization of β-bromo-α, β-unsaturated amides with terminal alkynes leading to (3Z)-3- alkylidenepyrrol-1-ones

β-Bromo-α,β-unsaturated amides are coupled and cyclized with terminal alkynes in DMF at 110 °C in the presence of a catalytic amount of CuI and amino acid along with a base to give the corresponding (3Z)-3-alkylidenepyrrol-1-ones in moderate to good yield