Cas 395061-47-9,Benzenesulfonamide, N-[[[(2Z)-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-butenyl]amino]carbon yl]-4-methyl-

395061-47-9

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Basic information

Product Name: Benzenesulfonamide, N-[[[(2Z)-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-butenyl]amino]carbon yl]-4-methyl-
Synonyms:
CAS NO:395061-47-9
Molecular Formula: C18H30N2O4SSi
Molecular Weight: 398.599
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: Benzenesulfonamide, N-[[[(2Z)-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-butenyl]amino]carbon yl]-4-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-[[[(2Z)-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-butenyl]amino]carbon yl]-4-methyl-(395061-47-9)
EPA Substance Registry System: Benzenesulfonamide, N-[[[(2Z)-4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-butenyl]amino]carbon yl]-4-methyl-(395061-47-9)

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: 395061-47-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 395061-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,5,0,6 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 395061-47:
(8*3)+(7*9)+(6*5)+(5*0)+(4*6)+(3*1)+(2*4)+(1*7)=159
159 % 10 = 9
So 395061-47-9 is a valid CAS Registry Number.

395061-47-9Upstream product

4083-64-1 Tosyl isocyanate

395061-47-9Downstream Products

395061-48-0 (Z)-N-[4-hydroxybut-2-enyl]-N'-(p-toluenesulfonyl)urea

395061-47-9Relevant academic research and scientific papers

Catalytic asymmetric intramolecular aminopalladation: Enantioselective synthesis of vinyl-substituted 2-oxazolidinones, 2-imidazolidinones, and 2-pyrrolidinones

Overman,Remarchuk

, p. 12 - 13 (2007/10/03)

A new catalytic asymmetric synthesis of five-membered nitrogen heterocycles is reported. This synthesis employs ferrocenyloxazoline palladacycles (FOP trifluoroacetate catalysts) 2 and 4 and proceeds by a catalytic cycle involving Pd(II) intermediates. Fo

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