Cas 878556-90-2,Acetamide, 2-chloro-N-[(1S,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-[[( S)-(4-methylphenyl)sulfinyl]amino]-4-phenylbutyl]-N-(phenylmethyl)-

878556-90-2

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Basic information

Product Name: Acetamide, 2-chloro-N-[(1S,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-[[( S)-(4-methylphenyl)sulfinyl]amino]-4-phenylbutyl]-N-(phenylmethyl)-
Synonyms:
CAS NO:878556-90-2
Molecular Formula: C33H45ClN2O3SSi
Molecular Weight: 613.336
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: Acetamide, 2-chloro-N-[(1S,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-[[( S)-(4-methylphenyl)sulfinyl]amino]-4-phenylbutyl]-N-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Acetamide, 2-chloro-N-[(1S,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-[[( S)-(4-methylphenyl)sulfinyl]amino]-4-phenylbutyl]-N-(phenylmethyl)-(878556-90-2)
EPA Substance Registry System: Acetamide, 2-chloro-N-[(1S,2R)-1-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-2-[[( S)-(4-methylphenyl)sulfinyl]amino]-4-phenylbutyl]-N-(phenylmethyl)-(878556-90-2)

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: 878556-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 878556-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,5,5 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 878556-90:
(8*8)+(7*7)+(6*8)+(5*5)+(4*5)+(3*6)+(2*9)+(1*0)=242
242 % 10 = 2
So 878556-90-2 is a valid CAS Registry Number.

878556-90-2Upstream product

878556-90-2Downstream Products

878556-90-2Relevant academic research and scientific papers

Synthesis of highly substituted enantiopure piperazines and ketopiperazines from vicinal N-sulfinyl diamines

Viso, Alma,Fernandez De La Pradilla, Roberto,Flores, Aida,Garcia, Ana,Tortosa, Mariola,Lopez-Rodriguez, Maria L.

, p. 1442 - 1448 (2007/10/03)

Enantiopure 1-benzyl-2,3-disubstituted piperazines (4) have been synthesized by treatment of N-sulfinyl-N-benzyldiamino alcohols (1) with diethyl oxalate and sodium methoxide followed by reduction with borane. Alternatively, the sulfinamido group was pres

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