79204-89-0

Basic information

• Product Name: Benzenepropanamine, N-hydroxy-
• Synonyms: Benzenepropanamine, N-hydroxy-
• CAS NO: 79204-89-0
• Molecular Formula: C9H13NO
• Molecular Weight: 151.208
• Mol File: 79204-89-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenepropanamine, N-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanamine, N-hydroxy-(79204-89-0)
• EPA Substance Registry System: Benzenepropanamine, N-hydroxy-(79204-89-0)

Safety Data

• Hazardous Substances Data: 79204-89-0(Hazardous Substances Data)

Upstream product

• 300843-72-5 C₁₁H₁₂N₂O 
• 104-53-0 3-phenyl-propionaldehyde 
• 2038-57-5 3-Phenylpropan-1-amine 
• 154012-03-0 N-benzylidene-3-phenylpropylamine 
• 154582-41-9 2-((3-phenylpropyl)amino)acetonitrile 
• 1197-50-8 (E)-3-phenylpropionaldehyde oxime 
• 22818-69-5 (3-nitropropyl)benzene 

Downstream Products

• 635-46-1 1,2,3,4-tetrahydroisoquinoline 
• 82543-03-1 N-Hydroxy-N-(3-phenyl-propyl)-acetamide 
• 1401332-30-6 N¹-benzyl-N²-hydroxy-N²-(3-phenylpropyl)propane-1,2-diamine 
• 1197-50-8 (Z)-3-phenylpropionaldehyde oxime 
• 1197-50-8 (E)-3-phenylpropionaldehyde oxime 
• 1453196-54-7 (R)-N¹-benzyl-N²-hydroxy-N²-(3-phenylpropyl)propane-1,2-diamine 
• 1453196-53-6 (S)-N¹-benzyl-N²-hydroxy-N²-(3-phenylpropyl)propane-1,2-diamine 
• 1417406-96-2 C₂₁H₂₃NO₅ 
• 851228-87-0 3-((R)-2-{(1R,3aS,7aR)-4-[2-[(3S,5R)-3,5-Bis-(tert-butyl-dimethyl-silanyloxy)-2-methylene-cyclohex-(Z)-ylidene]-eth-(E)-ylidene]-7a-methyl-octahydro-inden-1-yl}-propyl)-5-methyl-2-(3-phenyl-propyl)-isoxazolidine-5-carboxylic acid methyl ester 
• 851228-86-9 C₄₄H₇₃NO₃Si₂ 

Relevant articles and documents

Facile reduction of nitroarenes into anilines and nitroalkanes into hydroxylamines via the rapid activation of ammonia· borane complex by supported gold nanoparticles

Gold nanoparticles supported on titania catalyse, even at a ppm loading level, the quantitative reduction of nitroarenes into anilines and nitroalkanes into alkylhydroxylamines by the ammonia× borane complex. No dehalohalogenation was seen in the case of chloro- or bromonitroarenes, while ester, cyano, or carboxylic acid functionalities also remain intact. The nitroarene to aniline reduction pathway does not require nitrosoarenes as intermediate products. Copyright

Practical synthesis and evaluation of the biological activities of 1α,25-dihydroxyvitamin D3 antagonists, 1α,25- dihydroxyvitamin D3-26,23-lactams. Designed on the basis of the helix 12-folding inhibition hypothesis

A practical synthetic route to novel vitamin D antagonists of DLAM (1α,25-dihydroxyvitamin D3-26,23-lactam) was developed from vitamin D2 via the 1,3-dipolar cycloaddition reaction as a key step. Six DLAM derivatives (24 compounds) w

Transformation of primary amines to N-monoalkylhydroxylamines: N-hydroxy-(S)-1-phenylethylamine oxalate: [(Benzenemethanamine, N-hydroxy--methyl-, (S)-, ethanedioate)]

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