124948-53-4

Basic information

• Product Name: N-Benzyliden-2-hydroxy-1-propanamin
• Synonyms: N-Benzyliden-2-hydroxy-1-propanamin
• CAS NO: 124948-53-4
• Molecular Weight: 163.219
• Mol File: 124948-53-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-Benzyliden-2-hydroxy-1-propanamin(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyliden-2-hydroxy-1-propanamin(124948-53-4)
• EPA Substance Registry System: N-Benzyliden-2-hydroxy-1-propanamin(124948-53-4)

Safety Data

• Hazardous Substances Data: 124948-53-4(Hazardous Substances Data)

Upstream product

• 6168-72-5 2-Amino-1-propanol 
• 100-52-7 benzaldehyde 
• 75-56-9 methyloxirane 
• 92-29-5 (E,E)-1,3,5-triphenyl-2,4-diazapenta-1,4-diene 

Downstream Products

• 55277-94-6 N-Benzyliden-2-hydroxy-1-propanamin-N-oxid 
• 127535-96-0 (2-Allyloxy-propyl)-[1-phenyl-meth-(E)-ylidene]-amine 
• 127536-06-5 (2-Allyloxy-propyl)-benzyl-amine 
• 1283595-87-8 2-[(E)-benzylideneamino]-1-phenylethan-1-ol 
• 1086234-95-8 2-Benzylidenamino-2-phenylaethanol 
• 1283595-82-3 (2Z,NE)-N-benzylidenebut-2-en-1-amine 
• 68003-55-4 (E)-N-allylbenzylideneimine 
• 57527-55-6 (E)-N-benzylidenebutan-1-amine 
• 27845-51-8 (E)-N-benzylidenepropan-2-amine 
• 7780-04-3 1-amino-2-propanol hydrochloride 
• 100-52-7 benzaldehyde 
• 27845-50-7 (E)-N-benzylidenebenzylamine 

Relevant articles and documents

1,3-Dipolar Cycloaddition of Imidate Ylides on Imino-Alcohols: Synthesis of New Imidazolones Using Solvent Free Conditions.

Imidates derived from α-amino esters as potential azomethine ylides, undergo 1,3-dipolar cycloaddition with imino-alcohols, in tautomeric equilibrium with 1,3-oxazolidines, without solvent at 70 deg C or under microwave irradiation.This reaction leads to a wide range of novel polyfunctionalized 4-yliden-2-imidazolin-5-ones in good yields with short reaction times.The reactivity of these imidates derived from α-amino esters with imino-alcohols is rationalized from the energy of the Frontier Molecular Orbitals (FMO) determined by semi-empirical PM3 calculations : the reaction is controlled by the interaction HOMO(1,3-dipole) - LUMO(dipolarophile) and the second order perturbation energy calculations are in agreement with the experimental reaction orientation.