Cas 123426-48-2,1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine

123426-48-2

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Basic information

Product Name: 1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine
Synonyms: 1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine
CAS NO:123426-48-2
Molecular Formula:
Molecular Weight: 381.539
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: 1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine(123426-48-2)
EPA Substance Registry System: 1-(4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-naphthalen-1-yl)-piperidine(123426-48-2)

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: 123426-48-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123426-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,2 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 123426-48:
(8*1)+(7*2)+(6*3)+(5*4)+(4*2)+(3*6)+(2*4)+(1*8)=102
102 % 10 = 2
So 123426-48-2 is a valid CAS Registry Number.

123426-48-2Upstream product

123426-48-2Downstream Products

123426-50-6 4-Methyl-2-phenylmethanesulfonyl-3,4-dihydro-2H-naphthalen-1-one

123426-48-2Relevant academic research and scientific papers

REACTION DU CHLORURE DE PHENYLMETHANESULFONYLE SUR QUELQUES ENAMINES DE TETRALONES-1: COMPETITION ENTRE CYCLOADDITIONS et RESULTATS PRELIMINAIRES

Kitane, Said,Vebrel, Joeel,Cerutti, Ernest,Berrada, Mohamed

, p. 109 - 112 (2007/10/02)

Enamines of 1-tetralones can react as enamine or (and) aminodiene with phenylsulfene.An unexpected competion occurs between cycloaddition and .This perticular behaviour is probably due to the benzocondensed nature of enamines.

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