688362-68-7

Basic information

• Product Name: (R)-(+)-N-acetyl-1-phenylprop-2-enylamine
• Synonyms: (R)-(+)-N-acetyl-1-phenylprop-2-enylamine
• CAS NO: 688362-68-7
• Molecular Weight: 175.23
• Mol File: 688362-68-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R)-(+)-N-acetyl-1-phenylprop-2-enylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-N-acetyl-1-phenylprop-2-enylamine(688362-68-7)
• EPA Substance Registry System: (R)-(+)-N-acetyl-1-phenylprop-2-enylamine(688362-68-7)

Safety Data

• Hazardous Substances Data: 688362-68-7(Hazardous Substances Data)

Upstream product

• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 59874-90-7 N-<1-(1-phenylprop-2-enyl)> trichloroacetamide 
• 59874-81-6 1-(1-imino-2,2,2-trichloroethoxy)-3-phenyl-2(E)-propene 
• 108-21-4 Isopropyl acetate 
• 4393-21-9 1-(phenyl)allylamine 
• 154614-38-7 (+/-)-N-1-acetyl-1-phenyl-2-propenylamine 
• 123772-66-7 N-(α-phenylpropargyl)acetamide 
• 676268-38-5 (1S,1'S)-(-)-N-(1-phenylbutoxy)-3-phenyl-3-prop-1-enylamine 
• 260998-33-2 (E)-(S)-(-)-O-(1-phenylbutyl) benzaldehyde oxime 
• 141-78-6 ethyl acetate 
• 108-24-7 acetic anhydride 

Downstream Products

• 688362-39-2 N-[(1R)-1-phenylprop-2-en-1-yl]benzamide 
• 103150-32-9 (1S,2R)-N-1-(1-phenyl-2,3-dihydroxypropyl)benzamide 
• 325490-29-7 (1R)-1-phenylprop-2-en-1-amine 

Relevant articles and documents

Enantioseparation, in vitro testing, and structural characterization of triple-binding reactivators of organophosphate-inhibited cholinesterases

The enantiomers of racemic 2-hydroxyimino-N-(azidophenylpropyl)acetamide-derived triple-binding oxime reactivators were separated, and tested for inhibition and reactivation of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibited with ta

Enantioselective synthesis of 1-aryl-2-propenylamines: A new approach to a stereoselective synthesis of the Taxol side chain

A variety of substituted 1-aryl-2-propenylamines of high enantiomeric purity were prepared via lipase-catalysed resolution of the corresponding racemates. (R)-1-Phenyl-2-propenylamine was further synthesised into (2R,3S)-3-benzoylamino-2-hydroxy-3-phenylpropanoic acid methyl ester, the side chain of Taxol.