Cas 548761-61-1,N-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide

548761-61-1

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Basic information

Product Name: N-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide
Synonyms: N-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide
CAS NO:548761-61-1
Molecular Formula:
Molecular Weight: 547.791
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-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide(548761-61-1)
EPA Substance Registry System: N-[4-(tert-butyl(diphenyl)silanyloxy)-1-(furan-2-yl)butyl]-4-methylbenzenesulfonamide(548761-61-1)

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: 548761-61-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 548761-61-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,7,6 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 548761-61:
(8*5)+(7*4)+(6*8)+(5*7)+(4*6)+(3*1)+(2*6)+(1*1)=191
191 % 10 = 1
So 548761-61-1 is a valid CAS Registry Number.

548761-61-1Upstream product

548761-61-1Downstream Products

548761-61-1Relevant academic research and scientific papers

A flexible approach toward trisubstituted piperidines and indolizidines: Synthesis of 6-epi-indolizidine 223A

Harris, Joel M.,Padwa, Albert

, p. 4371 - 4381 (2007/10/03)

2,5,6-Trisubstituted piperidines are readily prepared by a combination of an aza-Achmatowicz oxidation of a furyl-substituted benzenesulfonamide followed by a conjugate addition to the resulting 2H-pyridone and subsequent addition of various nucleophiles

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