72002-77-8

Basic information

• Product Name: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-
• CAS NO: 72002-77-8
• Molecular Formula: C16H17NO3
• Molecular Weight: 271.316
• Mol File: 72002-77-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-(72002-77-8)
• EPA Substance Registry System: Benzamide, N-[(1S,2S)-2-hydroxy-1-(hydroxymethyl)-2-phenylethyl]-(72002-77-8)

Safety Data

• Hazardous Substances Data: 72002-77-8(Hazardous Substances Data)

Upstream product

• 93-58-3 benzoic acid methyl ester 
• 28143-91-1 (1S,2S)-2-amino-1-phenyl-1,3-diol 
• 93-97-0 benzoic acid anhydride 
• 41542-84-1 N-(1-hydroxymethyl-2-oxo-2-phenyl-ethyl)-benzamide 
• 3313-16-4 (1RS,2RS)-2-benzoylamino-1,3-bis-benzoyloxy-1-phenyl-propane 
• 16735-23-2 3-hydroxy-1-oxo-1-phenylpropan-2-aminium chloride 
• 3313-16-4 (1RS,2SR)-2-benzoylamino-1,3-bis-benzoyloxy-1-phenyl-propane 
• 60083-18-3 3-oxo-3-phenyl-2-(phenylhydrazono)propanal 
• 4190-14-1 N-(2-oxo-2-phenylethyl)benzamide 
• 115964-09-5 (1RS:2SR)-2-benzamino-3-benzoyloxy-1-phenyl-propanol-⁽¹⁾ 
• 526214-15-3 4-benzoyl-2-phenyl-4H-oxazol-5-one 
• 74104-28-2 α-acetamido-β-hydroxypropiophenone 
• 108943-99-3 N-(1-acetoxy-3-oxo-3-phenylpropyl)acetamide 
• 100610-56-8 (1RS,2RS)-1,3-diacetoxy-2-amino-1-phenyl-propane; hydrochloride 

Downstream Products

• 548773-02-0 4-Nitro-benzoic acid (R)-phenyl-((S)-2-phenyl-4,5-dihydro-oxazol-4-yl)-methyl ester 
• 3313-16-4 (1RS,2RS)-2-benzoylamino-1,3-bis-benzoyloxy-1-phenyl-propane 
• 101734-34-3 (RS)-4-((RS)-α-acetoxy-benzyl)-2-phenyl-4,5-dihydro-oxazole 
• 102012-91-9 (1RS,2RS)-1,3-diacetoxy-2-benzoylamino-1-phenyl-propane 
• 3306-06-7 (+/-)-threo-2-amino-1-phenyl-1,3-propanediol 
• 440643-35-6 [(S,S)-2-phenyl-4,5-dihydro-oxazol-4-yl]-phenyl-methanol 
• 102012-91-9 (1S,2S)-1,3-diacetoxy-2-benzoylamino-1-phenyl-propane 

Relevant articles and documents

Evaluation of chiral oxazolines for the highly enantioselective diethylzinc addition to N-(diphenylphosphinoyl) imines

On the basis of the principle that the incorporation of the structurally rigid and conformationally restricted skeleton in β-amino alcohols is beneficial to the enantioselective diethylzinc addition to imines, a series of chiral oxazolines, which had been

1,2-Asymmetric induction in conjugate addition of nitroalkenes

Conjugate addition of nucleophiles to the nitroalkenes 8 and 11 followed by in situ ozonolysis resulted in the formation of α-substituted thioesters exhibiting the 'unexpected' syn relative configuration between the C-3 and newly formed stereogenic centre