Cas 405176-15-0,Benzenesulfonamide, N-[(1R,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-hydroxy-2-( 4-nitrophenyl)ethyl]-4-methyl-

405176-15-0

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Basic information

Product Name: Benzenesulfonamide, N-[(1R,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-hydroxy-2-( 4-nitrophenyl)ethyl]-4-methyl-
Synonyms:
CAS NO:405176-15-0
Molecular Formula: C22H32N2O6SSi
Molecular Weight: 480.657
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-[(1R,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-hydroxy-2-( 4-nitrophenyl)ethyl]-4-methyl-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-[(1R,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-hydroxy-2-( 4-nitrophenyl)ethyl]-4-methyl-(405176-15-0)
EPA Substance Registry System: Benzenesulfonamide, N-[(1R,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-hydroxy-2-( 4-nitrophenyl)ethyl]-4-methyl-(405176-15-0)

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: 405176-15-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 405176-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,5,1,7 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 405176-15:
(8*4)+(7*0)+(6*5)+(5*1)+(4*7)+(3*6)+(2*1)+(1*5)=120
120 % 10 = 0
So 405176-15-0 is a valid CAS Registry Number.

405176-15-0Upstream product

405176-15-0Downstream Products

405176-17-2 (2S,3S)-2-hydroxymethyl-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)aziridine

405176-15-0Relevant academic research and scientific papers

Solution- and solid-phase synthesis of 4-hydroxy-4,5-dihydroisoxazole serivatives from enantiomerically pure N-tosyl-2,3-aziridine alcohols

Righi, Paolo,Scardovi, Noemi,Marotta, Emanuela,Holte, Peter Ten,Zwanenburg, Binne

, p. 497 - 500 (2002)

(formula presented) Enantiomerically pure N-tosyl-2,3-aziridine alcohols are directly converted into 4-hydroxy-4,5-dihydroisoxazole 2-oxides through oxidation to the corresponding aldehydes followed by in situ tandem nitroaldol-intramolecular cyclization.

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