852202-45-0

Basic information

• Product Name: (2R)-2-phenyl-2-[(1'R)-1'-(isopropyl)but-3'-enylamino]ethanol
• Synonyms: (2R)-2-phenyl-2-[(1'R)-1'-(isopropyl)but-3'-enylamino]ethanol
• CAS NO: 852202-45-0
• Molecular Weight: 233.354
• Mol File: 852202-45-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R)-2-phenyl-2-[(1'R)-1'-(isopropyl)but-3'-enylamino]ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R)-2-phenyl-2-[(1'R)-1'-(isopropyl)but-3'-enylamino]ethanol(852202-45-0)
• EPA Substance Registry System: (2R)-2-phenyl-2-[(1'R)-1'-(isopropyl)but-3'-enylamino]ethanol(852202-45-0)

Safety Data

• Hazardous Substances Data: 852202-45-0(Hazardous Substances Data)

Upstream product

• 852202-19-8 (R)-2-[2-Methyl-prop-(E)-ylideneamino]-2-phenyl-ethanol 
• 106-95-6 allyl bromide 
• 56613-80-0 D-2-phenylglycinol 

Downstream Products

• 1011296-26-6 (R)-N-[(R)-2-(tert-butyldimethylsilyloxy)-1-phenylethyl]-5-methylhex-1-en-4-amine 
• 434307-00-3 (R)-3-[(R)-2-methylhex-5-en-3-yl]-4-phenyloxazolidin-2-one 
• 4383-23-7 1-phenyl-but-3-enylamine 

Relevant articles and documents

Access to optically pure nitrogen heterocycles based on hydrozirconation of unsaturated secondary amines

Optically active N-heterocycles with four-, five-, or six-membered rings can be prepared from unsaturated secondary amines, by using a one-pot hydrozirconation/iodination sequence as the key step. The presented method allows the preparation of 2-substituted pyrrolidines enantiomeric to those previously obtained from N-allyloxazolidines. The two approaches use the same reagents (allyl bromide and aldehydes) and the same (R)-2-phenyl-glycinol as the chiral inductor. Georg Thieme Verlag Stuttgart.

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