124368-83-8

Basic information

• Product Name: (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane
• Synonyms: (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane
• CAS NO: 124368-83-8
• Molecular Weight: 265.471
• Mol File: 124368-83-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane(124368-83-8)
• EPA Substance Registry System: (1R,2S)-(-)-2-Amino-1-phenyl-1-<(tert-butyldimethylsilyl)oxy>-propane(124368-83-8)

Safety Data

• Hazardous Substances Data: 124368-83-8(Hazardous Substances Data)

Upstream product

• 120390-75-2 (R)-(+)-α-<(tert-butyldimethylsilyl)oxy>-benzeneacetonitrile 
• 492-41-1 (1R,2S)-norephedrine 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 1415568-35-2 C₁₇H₂₉NO₂Si 
• 1415568-44-3 C₁₇H₂₆⁽²⁾H₃NO₂Si 
• 3198-15-0 (1R,2S)-(-)-norephedrine hydrochloride 
• 138715-28-3 (4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone 
• 138715-29-4 (4S,5R)-3-<5-(1,2-dithiolan-3-yl)-1-oxopentyl>-4-methyl-5-phenyloxazolidine-2-selone 
• 138715-26-1 (1S,2R)-2-(tert-butyldimethylsiloxy)-1-methyl-2-phenylethyl isocyanide 
• 138715-27-2 (1S,2R)-2-(tert-butyldimethylsiloxy)-1-methyl-2-phenylethyl isoselenocyanate 
• 84025-82-1 (-)-(2R,3S)-3-Methyl-2-phenylmorpholin 
• 263143-80-2 N-[(1'S,2'R)-2'-tert-butyldimethylsiloxy-1'-methyl-2'-phenylethyl]piperidin-4-one 

Relevant articles and documents

Enhanced diastereoselectivity via confinement: Photoisomerization of 2,3-diphenylcyclopropane-1-carboxylic acid derivatives within zeolites

From the perspective of asymmetric induction, the photochemistry of 24 chiral esters and amides of cis-2,3-diphenylcyclopropane-1-carboxylic acid from excited singlet and triplet states has been investigated within zeolites. The chiral auxiliaries placed

Synthesis of (4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone: A Chiral Auxiliary Reagent Capable of Detecting the Enantiomers of (R,S)-Lipoic Acid by 77Se Nuclear Magnetic Resonance Spectroscopy

(4S,5R)-(-)-4-Methyl-5-phenyloxazolidine-2-selone was constructed in 5 steps on the 10-gram scale. 77Se NMR spectroscopic studies revealed that this selone served as a remarkably sensitive chiral auxiliary agent which readily distinguished the selone-coup