114655-48-0

Basic information

• Product Name: (E)-2-methyl-N-((E)-3-phenylallylidene)propan-2-amine
• Synonyms: (E)-2-methyl-N-((E)-3-phenylallylidene)propan-2-amine
• CAS NO: 114655-48-0
• Molecular Weight: 187.285
• Mol File: 114655-48-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: (E)-2-methyl-N-((E)-3-phenylallylidene)propan-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-methyl-N-((E)-3-phenylallylidene)propan-2-amine(114655-48-0)
• EPA Substance Registry System: (E)-2-methyl-N-((E)-3-phenylallylidene)propan-2-amine(114655-48-0)

Safety Data

• Hazardous Substances Data: 114655-48-0(Hazardous Substances Data)

Upstream product

• 118149-94-3 N-cinnamyl-N-t-butylhydroxyamine 
• 14371-10-9 (E)-3-phenylpropenal 
• 75-64-9 tert-butylamine 

Downstream Products

• 939-23-1 p-phenylpyridine 
• 2052-92-8 3-methyl-4-phenyl-pyridine 
• 14371-10-9 (E)-3-phenylpropenal 
• 99564-46-2 N-(tert-butyl)-3-phenyl-2-propenamide 
• 129959-63-3 1-tert-butyl-5-(α-chlorobenzyl)-7-chloromethyl-6-thiaisoheptanam 
• 129959-64-4 (1R,5R)-6-tert-Butyl-2-chloromethyl-4-(hydroxy-phenyl-methyl)-3-thia-6-aza-bicyclo[3.2.0]heptan-7-one 
• 129959-71-3 1-tert-butyl-3-chloro-5-(α-chlorobenzyl)-6-thiaisoheptanam 
• 129959-72-4 1-tert-butyl-5-chloro-3-chloromethyl-6-phenyl-7-thiaisoheptanam 
• 7749-92-0 diethyl 2-formyl-1-phenylethylphosphonate 
• 69139-24-8 (Z)-4-((E)-3-phenylallylidene)isochromane-1,3-dione 
• 90331-02-5 (Z)-N-(E)-3-phenylallylidene-t-butanamine oxide 
• 90330-97-5 (E)-2-(tert-butyl)-3-styryl-1,2-oxaziridine 
• 129959-70-2 1-tert-butyl-3-methylene-4-styrylazetidin-2-one 
• 84355-63-5 1-tert-Butyl-2-oxo-4-phenyl-1,2-dihydro-pyridine-3-carbonitrile 

Relevant articles and documents

Insertion of Nitriles into Zirconocene 1-aza-1,3-diene Complexes: Chemoselective Synthesis of N-H and N-Substituted Pyrroles

The direct insertion of nitriles into zirconocene-1-aza-1,3-diene complexes provides an efficient, chemoselective, and controllable synthesis of N-H and N-substituted pyrroles upon acidic aqueous work-up. The outcome of the reaction (that is, the formatio

Eco-friendly synthesis of imines by ultrasound irradiation

A series of imines was synthesized by an ultrasound-assisted reaction of aldehydes and primary amines using silica as the promoter. Products were obtained in high yields even in large scale synthesis.

One-pot synthesis of N-chloroacetyl 1-aminoalkyl phosphonates - Precursors of 4-phosphono-β-lactams

4-Phosphono-β-lactams are synthesized via a three-step sequence, including final formation of the C3-C4 bond through a phosphorus-stabilized carbanion. The chlorinated precursors can be synthesized via two different methods: a one-pot N-acylation of an aromatic imine followed by addition of a trialkyl phosphite or phosphonylation of a suitable imine followed by N-acylation in a separate reaction step. The former method was preferred because of the ease of the reaction and the good yields obtained. Georg Thieme Verlag Stuttgart.