Cas 333459-63-5,<i>N</i>-[1-(<i>tert</i>-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide

333459-63-5

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Basic information

Product Name: N-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide
Synonyms: N-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide
CAS NO:333459-63-5
Molecular Formula:
Molecular Weight: 551.822
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-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide(333459-63-5)
EPA Substance Registry System: N-[1-(tert-butyl-diphenyl-silanyloxymethyl)-3-hydroxymethyl-hex-5-enyl]-4-methyl-benzenesulfonamide(333459-63-5)

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: 333459-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 333459-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,4,5 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 333459-63:
(8*3)+(7*3)+(6*3)+(5*4)+(4*5)+(3*9)+(2*6)+(1*3)=145
145 % 10 = 5
So 333459-63-5 is a valid CAS Registry Number.

333459-63-5Upstream product

333459-63-5Downstream Products

333459-64-6 N-[3-(tert-butyl-dimethyl-silanyloxymethyl)-1-(tert-butyl-diphenyl-silanyloxymethyl)-hex-5-enyl]-4-methyl-benzenesulfonamide

333459-63-5Relevant academic research and scientific papers

The iodocyclization of unsaturated dihydroxysulfonamide derivatives. N- versus O-cyclization

Cossy, Janine,Tresnard, Ludovic,Belotti, Damien,Pardo, Domingo Gomez

, p. 251 - 254 (2001)

Iodocyclization of unsaturated dihydroxysulfonamide derivatives can lead to substituted monocyclic or bicyclic compounds depending on the hydroxy protecting groups and the electrophilic reagent used.

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