33234-48-9

Basic information

• Product Name: 2-benzyl-1H-pyrrole
• CAS NO: 33234-48-9
• Molecular Formula: C₁₁H₁₁N
• Molecular Weight: 157.2117
• Mol File: 33234-48-9.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 281.7°C at 760 mmHg
• Flash Point: 114.9°C
• Density: 1.068g/cm³
• Vapor Pressure: 0.006mmHg at 25°C
• Refractive Index: 1.594
• CAS DataBase Reference: 2-benzyl-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyl-1H-pyrrole(33234-48-9)
• EPA Substance Registry System: 2-benzyl-1H-pyrrole(33234-48-9)

Safety Data

• Hazardous Substances Data: 33234-48-9(Hazardous Substances Data)

Upstream product

• 7697-46-3 phenyl(1H-pyrrol-2-yl)methanone 
• 10048-64-3 (E)-1-phenylpropan-2-one oxime 
• 74-86-2 acetylene 
• 109-97-7 pyrrole 
• 100-39-0 benzyl bromide 
• 10575-94-7 N-benzyl-N-nitrosobenzamide 
• 86688-89-3 1-(Phenylsulfonyl)-2-benzoylpyrrole 
• 130408-97-8 2-(1-hydroxybenzyl)-1-(triisopropylsilyl)pyrrole 

Downstream Products

• 92012-23-2 2-(4-Methoxybenzoyl)-5-benzylpyrrole 
• 92012-34-5 Methyl 5-benzylpyrrole-2-carboxylate 
• 92012-38-9 (2R,5S)-5-Benzyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 92012-27-6 (2S,5R)-2-Benzyl-5-(4-methoxy-benzoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 92012-40-3 cis-Methyl 5-benzylprolinate trifluoroacetate 
• 92012-31-2 2-<4-(Benzyloxy)benzoyl>-5-benzylpyrrolidine trifluoroacetic acid salt 
• 92012-29-8 trans-1-(tert-Butoxycarbonyl)-2-<4-(benzyloxy)benzoyl>-5-benzylpyrrolidine 
• 92012-28-7 cis-1-(tert-Butoxycarbonyl)-2-<4-(benzyloxy)benzoyl>-5-benzylpyrrolidine 
• 32648-97-8 (C₆H₅CH₂C₄H₄N)Cr(CO)3 

Relevant articles and documents

GRP94 SELECTIVE INHIBITORS AND USES THEREOF

The present technology provides compounds according to Formula I or Formula III as well as compositions including such compounds useful for the treatment of metastatic cancer and/or glaucoma.

An efficient one-pot synthesis of 2-benzylpyrroles and 3-benzylindoles

One-pot regioselective benzylation of pyrroles and indoles using zirconium tetrachloride is discussed. This has been achieved by in-situ generation of di(1H-pyrrol-1-yl)zirconium(IV) chloride and di(1H-indol-1-yl)zirconium(IV) chloride. It was observed th

Mono- and dialkylations of pyrrole at C2 and C5 positions by nucleophilic substitution reaction in ionic liquid

(Chemical Equation Presented) A novel ionic liquid methodology for pyrrole C-alkylation is described. The pyrrole alkylation is achieved with various simple alkyl halides and mesylates selectively at C2 and C5 positions in good yields with minimal byproducts under relatively mild conditions in various ionic liquids. 2-(3-Phenylpropyl)pyrrole (2a) was synthesized from pyrrole and 1-bromo-3-phenylpropane in a mixture solvent system, [bmim][SbF6] and CH3CN, in 81% yield at 115°C for 44 h with 5% yield of dialkylated compound 3a.