96422-88-7

Basic information

• Product Name: (1S,2S)-N-<2-(1H-Indol-3-yl)ethyl>-1-(hydroxymethyl)cyclohex-4-ene-2-acetamide
• Synonyms: (1S,2S)-N-<2-(1H-Indol-3-yl)ethyl>-1-(hydroxymethyl)cyclohex-4-ene-2-acetamide
• CAS NO: 96422-88-7
• Molecular Weight: 312.412
• Mol File: 96422-88-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (1S,2S)-N-<2-(1H-Indol-3-yl)ethyl>-1-(hydroxymethyl)cyclohex-4-ene-2-acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-N-<2-(1H-Indol-3-yl)ethyl>-1-(hydroxymethyl)cyclohex-4-ene-2-acetamide(96422-88-7)
• EPA Substance Registry System: (1S,2S)-N-<2-(1H-Indol-3-yl)ethyl>-1-(hydroxymethyl)cyclohex-4-ene-2-acetamide(96422-88-7)

Safety Data

• Hazardous Substances Data: 96422-88-7(Hazardous Substances Data)

Upstream product

• 96422-86-5 2-[(1S,6S)-6-((S)-1,2-Dihydroxy-ethyl)-cyclohex-3-enyl]-N-[2-(1H-indol-3-yl)-ethyl]-acetamide 
• 96422-84-3 Acetic acid (1S,4aS,8aS)-3-oxo-3,4,4a,5,8,8a-hexahydro-1H-isochromen-1-ylmethyl ester 
• 96422-83-2 Acetic acid (1S,4aS,8aS)-1-(4a,5,8,8a-tetrahydro-1H-isochromen-1-yl)methyl ester 
• 79849-65-3 (1S,2S,7R,9R)-10,12-dioxatricyclo[7.2.1.0^2,7]dodec-4-en-8-one 
• 96422-85-4 (1S,4aS,8aS)-1-Hydroxymethyl-1,4,4a,5,8,8a-hexahydro-isochromen-3-one 
• 96422-82-1 (1S,4aS,8aS)-1-(4a,5,8,8a-Tetrahydro-1H-isochromen-1-yl)-methanol 
• 22259-53-6 3-aminomethylindole 
• 61-54-1 tryptamine 
• 108098-51-7 (4aS,8aS)-1,4,4a,5,8,8a-Hexahydro-3H-2-benzopyran-3-one 
• 96422-87-6 2-((1S,6S)-6-Formyl-cyclohex-3-enyl)-N-[2-(1H-indol-3-yl)-ethyl]-acetamide 

Downstream Products

• 96422-89-8 2-((1S,6S)-6-Chloromethyl-cyclohex-3-enyl)-N-[2-(1H-indol-3-yl)-ethyl]-acetamide 
• 483-26-1 (-)-alloyohimbane 

Relevant articles and documents

First Enantioselective Synthesis of (-)-Akagerine by a Chemoenzymatic Approach

(-)-Akagerine (1) was synthesized in an efficient and stereocontrolled fashion from the readily available (1S,2R)-cyclohexenedimethanol monoacetate 4.Key steps were the cleavage of the C(17)/C(18) bond of a 14a and the regio- and stereoselective cyclizati