Cas 960004-40-4,4-methyl-N-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide

960004-40-4

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Basic information

Product Name: 4-methyl-N-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide
Synonyms: 4-methyl-N-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide
CAS NO:960004-40-4
Molecular Formula:
Molecular Weight: 482.503
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-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-methyl-N-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide(960004-40-4)
EPA Substance Registry System: 4-methyl-N-{(1S)-3-(phenylseleno)-1-[(tetrahydro-2H-pyran-2-yloxy)methyl]propyl}benzenesulfonamide(960004-40-4)

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: 960004-40-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 960004-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,0,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 960004-40:
(8*9)+(7*6)+(6*0)+(5*0)+(4*0)+(3*4)+(2*4)+(1*0)=134
134 % 10 = 4
So 960004-40-4 is a valid CAS Registry Number.

960004-40-4Upstream product

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960004-40-4Relevant academic research and scientific papers

Stereocontrolled synthesis of substituted N-arenesulfonyl azetidines from γ-(phenylseleno)alkyl arylsulfonamides

Tiecco, Marcello,Testaferri, Lorenzo,Temperini, Andrea,Terlizzi, Raffaella,Bagnoli, Luana,Marini, Francesca,Santi, Claudio

, p. 3510 - 3519 (2007)

Different synthetic methodologies for the stereocontrolled synthesis of substituted azetidines are reported. The approach utilizes an optimized oxidation reaction of γ-(phenylseleno)alkyl arylsulfonamides, followed by the intramolecular substitution of th

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