Cas 215923-82-3,N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide

215923-82-3

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Basic information

Product Name: N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide
Synonyms: N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide
CAS NO:215923-82-3
Molecular Formula:
Molecular Weight: 426.967
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: N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide(215923-82-3)
EPA Substance Registry System: N-[2-(8-Chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)-ethyl]-4-methyl-benzenesulfonamide(215923-82-3)

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: 215923-82-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 215923-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,9,2 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 215923-82:
(8*2)+(7*1)+(6*5)+(5*9)+(4*2)+(3*3)+(2*8)+(1*2)=133
133 % 10 = 3
So 215923-82-3 is a valid CAS Registry Number.

215923-82-3Upstream product

215923-82-3Downstream Products

215923-82-3Relevant academic research and scientific papers

Synthesis of a C11 spiropiperidino derivative of 8-chloro-6,11- dihydro 5H-benzo[5,6]cyclohepta[1,2-b]pyridine

Afonso, Adriano,Kelly,Puar, Mohindar S.,McCombie, Stuart,McPhail, Andrew T.

, p. 7661 - 7664 (1998)

A method using N-tosyl aziridine for the synthesis of a spiropiperidine 2 (R=H) is described. Cleavage of the N-tosyl group of the intermediate 8 to form the spiropiperidinone 9 was found to proceed in high yield with conc. sulfuric acid. Acylated derivat

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