95105-20-7

Basic information

• Product Name: (2S,3R)-3-amino-4-phenylbutane-1,2-diol
• Synonyms: (2S,3R)-3-amino-4-phenylbutane-1,2-diol
• CAS NO: 95105-20-7
• Molecular Weight: 181.235
• Mol File: 95105-20-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2S,3R)-3-amino-4-phenylbutane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-3-amino-4-phenylbutane-1,2-diol(95105-20-7)
• EPA Substance Registry System: (2S,3R)-3-amino-4-phenylbutane-1,2-diol(95105-20-7)

Safety Data

• Hazardous Substances Data: 95105-20-7(Hazardous Substances Data)

Upstream product

• 152897-52-4 (S)-5-<(S)-2-phenyl-1-(N-tosylamino)ethyl>-1,3-dioxolane 
• 1207946-42-6 (S)-N-(2-phenylethylidene)-tert-butylsulfinamide 
• 114886-83-8 methyl (2S,3R)-3-amino-2-hydroxy-4-phenylbutanoate 
• 100-44-7 benzyl chloride 
• 1268240-92-1 (R)-N-((R)-1-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylethyl)-2-methylpropane-2-sulfinamide 
• 147915-00-2 (2S,3R)-3-azido-1,2-O-methylethylidene-4-phenylbutane-1,2-diol 
• 147914-98-5 (2R,3S)-1,2-O-methylethylidene-4-phenylbutane-1,2,3-triol 
• 591-51-5 phenyllithium 
• 23402-69-9 lithium diphenylcuprate 
• 147976-15-6 (2S,3R)-3-azido-4-phenylbutane-1,2-diol 

Downstream Products

• 59969-65-2 (2S,3R)-3-benzyloxycarbonylamino-2-hydroxy-4-phenyl-butanoic acid 
• 124782-04-3 methyl (2S,3R)-3--2-hydroxy-4-phenylbutanoate 
• 100564-98-5 (4R,5S)-4-benzyl-2-oxo-5-oxazolidinecarboxylic acid 
• 95832-38-5 methyl (4R,5S)-2-oxo-4-phenylmethyl-1,3-oxazolidine-5-carboxylate 
• 147915-06-8 ethyl 4R <4β,5α(E)>-2-oxo-4-(phenylmethyl)oxazolidine-5-propenoate 
• 147915-03-5 (4R,5S)-5-hydroxy-4-phenylmethyl-3,4,5,6-tetrahydro-2H-1,3-oxazin-2-one 
• 95832-37-4 (4R,5S)-5-benzyl-4-(hydroxymethyl)-1,3-oxazolidin-2-one 
• 152897-53-5 (2S,3R)-3-benzyloxycarbonylamino-2-hydroxy-4-phenyl-1-butanol 

Relevant articles and documents

Total synthesis of (-)-Haouamine B pentaacetate and structural revision of haouamine B

The enantiocontrolled total synthesis of (-)-haouamine B pentaacetate was accomplished via an optically active indane-fused β-lactam, which was prepared by a newly developed Friedel-Crafts reaction. Subsequent cleavage of the β-lactam and an intramolecular McMurry coupling reaction provided the core indane-fused tetrahydropyridine, which led to the elucidation of the structure, as proposed by Trauner and Zuba.

Ring opening of optically active cis-disubstituted aziridino alcohols: An enantiodivergent synthesis of functionalized amino alcohol derivatives

Ring-opening reactions of optically active cis-disubstituted aziridino alcohols have been investigated. Regio- and stereo-selective ring opening took place with internal and external nucleophiles. Unusual amino acids derivatives (14) and (15), the key synthetic intermediates for bestatin and related peptides, have been prepared. n.

Enantiomerically pure 3-amino-2-hydroxy and 5-amino-4-hydroxy acids from D-isoascorbic acid

The chirospecific synthesis of 3-amino-2-hydroxy aldehyde or acid units is an important issue in the context of synthetic strategies directed towards the construction of biologically relevant target molecules such as amino sugars, antibiotics, enzyme inhi