Cas 143207-13-0,(3aS,5S,5aS,10bS,12bS)-6-Acetyl-3a-ethyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester

143207-13-0

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Basic information

Product Name: (3aS,5S,5aS,10bS,12bS)-6-Acetyl-3a-ethyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester
Synonyms:
CAS NO:143207-13-0
Molecular Formula:
Molecular Weight: 382.503
EINECS: N/A
Product Categories: N/A
Mol File: 143207-13-0.mol
Article Data: 1

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,5S,5aS,10bS,12bS)-6-Acetyl-3a-ethyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,5S,5aS,10bS,12bS)-6-Acetyl-3a-ethyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester(143207-13-0)
EPA Substance Registry System: (3aS,5S,5aS,10bS,12bS)-6-Acetyl-3a-ethyl-2,3,3a,4,5,5a,6,11,12,12b-decahydro-1H-6,12a-diaza-indeno[7,1-cd]fluorene-5-carboxylic acid methyl ester(143207-13-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 143207-13-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 143207-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 143207-13:
(8*1)+(7*4)+(6*3)+(5*2)+(4*0)+(3*7)+(2*1)+(1*3)=90
90 % 10 = 0
So 143207-13-0 is a valid CAS Registry Number.

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143207-13-0Relevant articles and documents

Reduction and N-alkylation of α-methylene-indolines with sodium cyanoborohydride in carboxylic acids

Balogh,Zsadon,Csampai,Pal

, p. 701 - 707 (1994)

The reaction of α-methylene-indolines with NaCNBH3 in carboxylic acids at room temperature can yield either 2β,3β-dihydro-indolines or their N- alkyl derivatives as main products with high selectively, depending mainly on the carboxylic acid and on the reaction time when using a large excess of NaCNBH3.

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