Cas 113807-83-3,(3aS,4R,5R,11bR)-5-(2-Benzenesulfinyl-acetyl)-4-ethyl-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester

113807-83-3

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Basic information

Product Name: (3aS,4R,5R,11bR)-5-(2-Benzenesulfinyl-acetyl)-4-ethyl-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester
Synonyms:
CAS NO:113807-83-3
Molecular Formula:
Molecular Weight: 464.585
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: (3aS,4R,5R,11bR)-5-(2-Benzenesulfinyl-acetyl)-4-ethyl-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,5R,11bR)-5-(2-Benzenesulfinyl-acetyl)-4-ethyl-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester(113807-83-3)
EPA Substance Registry System: (3aS,4R,5R,11bR)-5-(2-Benzenesulfinyl-acetyl)-4-ethyl-2,3,3a,4,5,7-hexahydro-1H-pyrrolo[2,3-d]carbazole-6-carboxylic acid methyl ester(113807-83-3)

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: 113807-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113807-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,8,0 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 113807-83:
(8*1)+(7*1)+(6*3)+(5*8)+(4*0)+(3*7)+(2*8)+(1*3)=113
113 % 10 = 3
So 113807-83-3 is a valid CAS Registry Number.

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113807-83-3Relevant academic research and scientific papers

AN ENANTIOSELECTIVE ACCESS TO THE (-)-TUBOTAIWINE SKELETON

Legseir, Belgacem,Henin, Jacques,Massiot, Georges,Vercauteren, Joseph

, p. 3573 - 3576 (2007/10/02)

An efficient induction of chirality is obtained when using α-phenylethylamine as a chiral starting material to produce in few steps the skeleton of anilinoacrylic indole alkaloids.Ring enlargement is described to produce the complete five-ring system of tubotaiwine.

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