166537-88-8

Basic information

• Product Name: 2-(bromomethyl)-5-phenyl-3,4-dihydro-2H-pyrrole
• Synonyms: 2-(bromomethyl)-5-phenyl-3,4-dihydro-2H-pyrrole
• CAS NO: 166537-88-8
• Molecular Weight: 238.127
• Mol File: 166537-88-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(bromomethyl)-5-phenyl-3,4-dihydro-2H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(bromomethyl)-5-phenyl-3,4-dihydro-2H-pyrrole(166537-88-8)
• EPA Substance Registry System: 2-(bromomethyl)-5-phenyl-3,4-dihydro-2H-pyrrole(166537-88-8)

Safety Data

• Hazardous Substances Data: 166537-88-8(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 3240-29-7 1-Phenylpent-4-en-1-one 
• 59239-04-2 1-phenyl-4-penten-1-one oxime 
• 7103-09-5 4-but-1-enylmagnesium bromide 
• 100-47-0 benzonitrile 

Downstream Products

• 1106994-59-5 C₁₁H₁₁BrFN 
• 1106994-00-6 5-(bromomethyl)-3,3-difluoro-2-phenyl-1-pyrroline 
• 853208-84-1 5-(bromomethyl)-3,3-dichloro-2-phenyl-1-pyrroline 

Relevant articles and documents

Synthesis of Functionalized Pyrrolines via Microwave-Promoted Iminyl Radical Cyclizations

O-Phenyloximes tethered to alkenes undergo 5-exo-trig iminyl radical cyclizations upon microwave irradiation. Trapping of the resulting cyclic radicals results in C-C, C-N, C-O, C-S, or C-X bond formation. Allylic sulfides undergo a tandem cyclization-thi

New synthesis of 3-fluoropyrroles

5-Alkoxymethyl-2-aryl-3-fluoro-1H-pyrroles and 2-aryl-3-fluoro-1H-pyrrole- 5-carbaldehydes were efficiently prepared from the corresponding 2-aryl-5-(bromomethyl)-1-pyrrolines via electrophilic α, α-difluorination of the imino bond, using Selectfluor (1-c

Synthesis of dihydropyrrole derivatives by copper-catalyzed cyclization of γ, δ-unsaturated ketone O-methoxycarbonyloximes

2-Bromomethyl-3,4-dihydro-2H-pyrroles are prepared from γ, δ-unsaturated ketone O-methoxycarbonyloximes by treatment with a catalytic amount of CuBr·SMe2 and LiBr.