566949-99-3

Basic information

• Product Name: (R)-[(R)-2-methoxy-1-phenylethyl]-(1-phenylbuta-2,3-dienyl)amine
• Synonyms: (R)-[(R)-2-methoxy-1-phenylethyl]-(1-phenylbuta-2,3-dienyl)amine
• CAS NO: 566949-99-3
• Molecular Weight: 279.382
• Mol File: 566949-99-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (R)-[(R)-2-methoxy-1-phenylethyl]-(1-phenylbuta-2,3-dienyl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-[(R)-2-methoxy-1-phenylethyl]-(1-phenylbuta-2,3-dienyl)amine(566949-99-3)
• EPA Substance Registry System: (R)-[(R)-2-methoxy-1-phenylethyl]-(1-phenylbuta-2,3-dienyl)amine(566949-99-3)

Safety Data

• Hazardous Substances Data: 566949-99-3(Hazardous Substances Data)

Upstream product

• 144302-38-5 (R)-benzylidene-(2-methoxy-1-phenylethyl)amine 
• 106-96-7 propargyl bromide 

Downstream Products

• 1088610-45-0 C₁₉H₂₁NO 
• 566950-11-6 (+)-(R)-1-phenylbuta-2,3-dien-1-ylamine 
• 2941-19-7 (R)-1-phenylbutylamine 
• 566950-10-5 (R)-2-Phenyl-2-((R)-1-phenyl-buta-2,3-dienylamino)-ethanol 

Relevant articles and documents

Asymmetric synthesis of allyl- and α-allenylamines from chiral imines and alkynes via (η2-imine)Ti(O-i-Pr)2 complexes

(Matrix presented) The reaction of a divalent titanium reagent Ti(O-i-Pr)4/2i-PrMgX with optically active arylaldimines derived from arylaldehydes and O-methylphenylglycinol provided, in a highly diastereoselective manner, chiral (η2-imine)Ti(O-i-Pr) 2 complexes, which in turn reacted with 1-alkynes or propargyl compounds to give optically active allyl- and α-allenylamines, respectively.