Cas 1357007-91-0,ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate

1357007-91-0

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Basic information

Product Name: ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate
Synonyms: ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate
CAS NO:1357007-91-0
Molecular Formula:
Molecular Weight: 653.891
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: ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate(1357007-91-0)
EPA Substance Registry System: ethyl 3-((2R,3R,4R,5S)-3,4-bis(benzyloxy)-5-benzyloxymethyl-N-hydroxypyrrolidin-2-yl)-(3S)-3-(dimethylphenylsilyl)propanoate(1357007-91-0)

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: 1357007-91-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357007-91-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,0,0 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1357007-91:
(9*1)+(8*3)+(7*5)+(6*7)+(5*0)+(4*0)+(3*7)+(2*9)+(1*1)=150
150 % 10 = 0
So 1357007-91-0 is a valid CAS Registry Number.

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1357007-91-0Relevant academic research and scientific papers

SmI2-mediated cross-coupling of nitrones with β-silyl acrylates: Synthesis of (+)-Australine

Gilles, Pierre,Py, Sandrine

, p. 1042 - 1045 (2012)

The SmI2-mediated cross-coupling of nitrones with β-silyl-α,β-unsaturated esters, followed by zinc reduction, allows an efficient and highly diastereoselective preparation of β-silyl lactams, which are precursors of β-hydroxy lactams through Ta

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