Cas 634599-58-9,3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole

634599-58-9

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Basic information

Product Name: 3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole
Synonyms: 3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole
CAS NO:634599-58-9
Molecular Formula:
Molecular Weight: 506.666
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole(CAS DataBase Reference)
NIST Chemistry Reference: 3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole(634599-58-9)
EPA Substance Registry System: 3-[(1R,2R,3R,6S)-6-isopropenyl-3-methyl-2-(methoxycarbonyl)amino-3-vinylcyclohexyl]-1-tosyl-1H-indole(634599-58-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 634599-58-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 634599-58-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,5,9 and 9 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 634599-58:
(8*6)+(7*3)+(6*4)+(5*5)+(4*9)+(3*9)+(2*5)+(1*8)=199
199 % 10 = 9
So 634599-58-9 is a valid CAS Registry Number.

634599-58-9Upstream product

2065-66-9 methyl-triphenylphosphonium iodide

634599-58-9Downstream Products

634599-58-9Relevant academic research and scientific papers

The Total Synthesis of (+)-Hapalindole Q by an Organomediated Diels-Alder Reaction

Kinsman, Aaron C.,Kerr, Michael A.

, p. 14120 - 14125 (2003)

The total synthesis of (+)-hapalindole Q has been achieved. The key step is a Diels-Alder reaction mediated by MacMillan's organocatalyst to provide the critical intermediate with high enantiose-lectivity (93% ee). This step establishes the proper arrange

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