Cas 141812-92-2,(1R,3R,4S)-2-Benzyl-4-methyl-1-pyridin-2-yl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester

141812-92-2

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Basic information

Product Name: (1R,3R,4S)-2-Benzyl-4-methyl-1-pyridin-2-yl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester
Synonyms:
CAS NO:141812-92-2
Molecular Formula:
Molecular Weight: 411.503
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: (1R,3R,4S)-2-Benzyl-4-methyl-1-pyridin-2-yl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3R,4S)-2-Benzyl-4-methyl-1-pyridin-2-yl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(141812-92-2)
EPA Substance Registry System: (1R,3R,4S)-2-Benzyl-4-methyl-1-pyridin-2-yl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester(141812-92-2)

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: 141812-92-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141812-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,8,1 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141812-92:
(8*1)+(7*4)+(6*1)+(5*8)+(4*1)+(3*2)+(2*9)+(1*2)=112
112 % 10 = 2
So 141812-92-2 is a valid CAS Registry Number.

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141812-92-2Relevant academic research and scientific papers

STEREOSPECIFIC SYNTHESIS OF TRANS, CIS-1,3,4-TRISUBSTITUTED 1,2,3,4-TETRAHYDRO-β-CARBOLINES

Behforouz, Mohammad,West, Sarah J.,Chakrabarty, Chitra,Rusk, David A.,Zarrinmayeh, Hamideh

, p. 483 - 495 (2007/10/02)

Pictet-Spengler condensation of Nb-benzyl-β-methyltryptophan methyl ester (2RS,3SR;4) with aldehydes followed by debenzylation afforded trans, cis-1,3,4-trisubstituted 1,2,3,4-tetrahydro-β-carbolines in complete stereospecific fashion.Tetrahydr

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