112055-09-1

Basic information

• Product Name: Carbamic acid, [2-(2-propenylamino)ethyl]-, phenylmethyl ester
• CAS NO: 112055-09-1
• Molecular Formula: C13H18N2O2
• Molecular Weight: 234.298
• Mol File: 112055-09-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Carbamic acid, [2-(2-propenylamino)ethyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, [2-(2-propenylamino)ethyl]-, phenylmethyl ester(112055-09-1)
• EPA Substance Registry System: Carbamic acid, [2-(2-propenylamino)ethyl]-, phenylmethyl ester(112055-09-1)

Safety Data

• Hazardous Substances Data: 112055-09-1(Hazardous Substances Data)

Upstream product

• 53844-02-3 benzyl N-(2-bromoethyl)carbamate 
• 107-11-9 1-amino-2-propene 

Downstream Products

• 1007121-66-5 benzyl 2-(N-allyl-2,2,2-trifluoroacetamido)ethylcarbamate 
• 1007121-63-2 benzyl 2-(N-allyl-4-methylbenzenesulfonamido)ethylcarbamate 
• 112055-12-6 2-<2-<(carbobenzoxy)amino>ethyl>-cis-3a,4,5,9b-tetrahydro-6,7-dimethoxy-1H-benzisoindole-1(2H)-one 
• 112055-12-6 2-<2-<(carbobenzoxy)amino>ethyl>-trans-3a,4,5,9b-tetrahydro-6,7-dimethoxy-1H-benzisoindole-1(2H)-one 
• 112055-11-5 3,4-dimethoxy-N-allyl-N'-carbobenzoxybenzocyclobutane-1-carboxamide 

Relevant articles and documents

Palladium-catalyzed intramolecular chloroamination of alkenes

A mild and facile Pd-catalyzed intramolecular chloroamination of unactivated alkenes has been described. This reaction takes place at room temperature and is tolerant of synthetically useful acid-sensitive functional groups. Generally high exo-selectiviti

Synthesis of Hexahydro-5H-benzimidazoisoindole 2 via an Intramolecular Diels-Alder Reaction and a Novel Lawesson's Reagent Mediated Cyclization

The 2-(5,6-dihydroxy-1,2,3,4-tetrahydro-1-naphthyl)imidazoline 1 is a recently reported potent alpha-adrenergic agent .In continuation of our work on the synthesis of potential adrenergic agents we required imidazoisoindole 2 in order to investigate th