702684-12-6

Basic information

• Product Name: (-)-(βR)-β-{[(1E)-(2-methoxyphenyl)methylene]amino}benzeneethanol
• Synonyms: (-)-(βR)-β-{[(1E)-(2-methoxyphenyl)methylene]amino}benzeneethanol
• CAS NO: 702684-12-6
• Molecular Weight: 255.316
• Mol File: 702684-12-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (-)-(βR)-β-{[(1E)-(2-methoxyphenyl)methylene]amino}benzeneethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-(βR)-β-{[(1E)-(2-methoxyphenyl)methylene]amino}benzeneethanol(702684-12-6)
• EPA Substance Registry System: (-)-(βR)-β-{[(1E)-(2-methoxyphenyl)methylene]amino}benzeneethanol(702684-12-6)

Safety Data

• Hazardous Substances Data: 702684-12-6(Hazardous Substances Data)

Upstream product

• 56613-80-0 D-2-phenylglycinol 
• 135-02-4 ortho-anisaldehyde 

Downstream Products

• 123983-05-1 2?[(1R)?1-aminoethyl]phenol 
• 40023-74-3 (R)-1-(2-methoxyphenyl)ethylamine 
• 1020255-46-2 N-tert-butoxycarbonyl-1-(2'-methoxyphenyl)but-3-enamine 
• 936227-08-6 (R)-3-[(R)-1-(2-methoxyphenyl)but-3-enyl]-4-phenyloxazolidin-2-one 
• 852202-09-6 2-[1-(2-methoxy-phenyl)-but-3-enylamino]-2-phenyl-ethanol 
• 702684-14-8 (-)-(βR)-β-{[(1R)-(2-methoxyphenyl)ethyl]amino}benzeneethanol 

Relevant articles and documents

Indium-mediated asymmetric barbier-type allylation of aldimines in alcoholic solvents: Synthesis of optically active homoallylic amines

(Chemical Equation Presented) Chiral aldimines derived from phenylglycinol were diastereoselectively allylated with indium powder/allyl bromide in alcoholic solvents. Both aliphatic and aromatic aldimines provided good yield of the desired products with h