Cas 89209-41-6,4-[(1S,3S)-3-Cyano-2-(2,2,2-trifluoro-acetyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]-2,2-bis-phenylsulfanyl-butyric acid methyl ester

89209-41-6

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Basic information

Product Name: 4-[(1S,3S)-3-Cyano-2-(2,2,2-trifluoro-acetyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]-2,2-bis-phenylsulfanyl-butyric acid methyl ester
Synonyms:
CAS NO:89209-41-6
Molecular Formula:
Molecular Weight: 609.693
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: 4-[(1S,3S)-3-Cyano-2-(2,2,2-trifluoro-acetyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]-2,2-bis-phenylsulfanyl-butyric acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(1S,3S)-3-Cyano-2-(2,2,2-trifluoro-acetyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]-2,2-bis-phenylsulfanyl-butyric acid methyl ester(89209-41-6)
EPA Substance Registry System: 4-[(1S,3S)-3-Cyano-2-(2,2,2-trifluoro-acetyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]-2,2-bis-phenylsulfanyl-butyric acid methyl ester(89209-41-6)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 89209-41-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89209-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,0 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89209-41:
(7*8)+(6*9)+(5*2)+(4*0)+(3*9)+(2*4)+(1*1)=156
156 % 10 = 6
So 89209-41-6 is a valid CAS Registry Number.

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89209-41-6Relevant academic research and scientific papers

Synthesis of the Two Enantiomers of a Tetrahydro-β-carboline from L-(-)-Tryptophan

Massiot, Georges,Mulamba, Tshilundu

, p. 1147 - 1149 (2007/10/02)

Pictet-Spengler condensations of methyl 4-formyl-2,2-bis(phenylthio)butyrate with tryptophanamide and Nb-benzyltryptophanamide are stereospecific; dehydration of the adducts followed by cyanide elimination (NaBH4) yields tetrahydro-

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