Cas 114663-08-0,4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide

114663-08-0

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Basic information

Product Name: 4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide
Synonyms:
CAS NO:114663-08-0
Molecular Formula:
Molecular Weight: 483.653
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: 4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide(114663-08-0)
EPA Substance Registry System: 4-Methyl-N-phenylsulfanyl-N-[1-phenyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-benzenesulfonamide(114663-08-0)

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: 114663-08-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114663-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,6 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114663-08:
(8*1)+(7*1)+(6*4)+(5*6)+(4*6)+(3*3)+(2*0)+(1*8)=110
110 % 10 = 0
So 114663-08-0 is a valid CAS Registry Number.

114663-08-0Upstream product

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114663-08-0Relevant academic research and scientific papers

Structure Determination of Unusual Rearrangement Products of S-(1-Alkenyl)sulfoximides by Collisionally Activated Dissociation Mass Spectrometry (CAD-MS)

Veith, Hans-Juergen von,Gais, Hans-Joachim,Erdelmeier, Irene

, p. 1041 - 1049 (1987)

The molecular ions of S-(1-alkenyl)-N-sulfoximides 1 are transformed into the N-(phenylsulfenyl)sulfonamides 3+. by a 1,2-migration of the alkenyl group to the O-atom of the sulfoximide function followed by a 2,3-sigmatropic

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