Cas 81375-31-7,Toluene-4-sulfonate8-chloro-2-ethylamino-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-2-ium;

81375-31-7

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Basic information

Product Name: Toluene-4-sulfonate8-chloro-2-ethylamino-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-2-ium;
Synonyms:
CAS NO:81375-31-7
Molecular Formula:
Molecular Weight: 435.975
EINECS: N/A
Product Categories: N/A
Mol File: 81375-31-7.mol
Article Data: 2

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: Toluene-4-sulfonate8-chloro-2-ethylamino-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-2-ium;(CAS DataBase Reference)
NIST Chemistry Reference: Toluene-4-sulfonate8-chloro-2-ethylamino-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-2-ium;(81375-31-7)
EPA Substance Registry System: Toluene-4-sulfonate8-chloro-2-ethylamino-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indol-2-ium;(81375-31-7)

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: 81375-31-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81375-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,7 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81375-31:
(7*8)+(6*1)+(5*3)+(4*7)+(3*5)+(2*3)+(1*1)=127
127 % 10 = 7
So 81375-31-7 is a valid CAS Registry Number.

81375-31-7Upstream product

81375-31-7Downstream Products

81375-31-7Relevant articles and documents

Conversion of Tetrahydro-γ-carbolines into Hexahydrodiazepinoindoles via Ylide Intermediates. X-Ray Crystal Structure Determination of 9-Bromo-2,3-dimethyl-1,2,3,4,5,6-hexahydrodiazepinoindole

Tamura, Yasumitsu,Tsubouchi, Hidetsugu,Morita, Iwao,Ikeda, Hiroyuki,Ikeda, Masazumi,Kido, Masaru

, p. 1937 - 1939 (1983)

N-Amination of 2-methyl-2,3,4,5-tetrahydro-1H-pyridoindoles with N-alkyl-O-tosylhydroxylamines followed by base treatment gave 1,2,3,4,5,6-hexahydro-2,3-dialkyldiazepinoindoles, the structure of one of which was determined by spectrosco

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