25662-24-2

Basic information

• Product Name: Aziridine, 2-(bromomethyl)-1-(phenylmethyl)-
• CAS NO: 25662-24-2
• Molecular Formula: C10H12BrN
• Molecular Weight: 226.116
• Mol File: 25662-24-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Aziridine, 2-(bromomethyl)-1-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Aziridine, 2-(bromomethyl)-1-(phenylmethyl)-(25662-24-2)
• EPA Substance Registry System: Aziridine, 2-(bromomethyl)-1-(phenylmethyl)-(25662-24-2)

Safety Data

• Hazardous Substances Data: 25662-24-2(Hazardous Substances Data)

Upstream product

• 188818-01-1 N-benzylidene-2,3-dibromopropylamine 
• 100-52-7 benzaldehyde 
• 68003-55-4 (E)-N-allylbenzylideneimine 
• 68003-55-4 benzylidene allylamine 
• 156697-66-4 N-benzylidene-2,3-dibromopropan-1-amine 

Downstream Products

• 420820-69-5 2,3-dibromo-1-(N,N-dibenzylamino)propane 
• 883199-53-9 1-phenylmethyl-2-(3-chlorophenoxymethyl)aziridine 
• 915728-57-3 C₂₃H₃₀BrNO₂ 
• 915728-56-2 C₂₂H₂₇Br₂NO₂ 
• 952024-11-2 5-[bis(benzyl)amino]-4-bromopentanenitrile 
• 952024-06-5 1-benzyl-2-(2-cyanoethyl)-aziridine 
• 897440-34-5 1-benzyl-2-(cyanomethyl)aziridine 
• 27159-40-6 2-ethyl-1-(phenylmethyl)aziridine 
• 4383-22-6 Allylbenzylamine 
• 832724-78-4 1-phenylmethyl-2-(thiocyanatomethyl)aziridine 
• 27701-36-6 N-allyl-N-benzyl-N,N-dimethylammonium iodide 
• 188818-06-6 N-benzyl-2-methylene-aziridine 
• 31201-91-9 4-methyl-1-phenyl-2-aza-1,3-butadiene 

Relevant articles and documents

Coupling of 1-alkyl-2-(bromomethyl)aziridines with lithium dialkylcuprates towards 1,2-dialkylaziridines

The reactivity of 1-alkyl-2-(bromomethyl)aziridines with respect to lithium dialkylcuprates (Gilman reagents) has been evaluated for the first time, pointing to the conclusion that these substrates can be applied successfully as synthetic equivalents for

Mechanistic considerations for the consecutive cyclization of 2,3-dibromopropylamine hydrobromide giving a strained molecule, 1-azabicyclo[1.1.0]butane

The effective formation of 1-azabicyclo[1.1.0]butane (2) by treatment of 2,3-dibromopropylamine hydrobromide (1) with n-BuLi could be understood considering a rational reaction pathway via both transition states 10 and 19 based on the intramolecular Br...

Sonochemical Cleavage of 2-(Bromomethyl)aziridines by a Zinc-Copper Couple

1-Alkyl- and 1-arylmethyl-2-(bromomethyl)aziridines are readily cleaved by the sonochemical zinc-copper couple in aqueous methanol at room temp. to afford allylamines.