Cas 389807-13-0,5(4H)-Oxazolone, 4-[(1R,2E)-1-(acetyloxy)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-buten yl]-4-[(dimethylphenylsilyl)methyl]-2-phenyl-, (4R)-

389807-13-0

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Basic information

Product Name: 5(4H)-Oxazolone, 4-[(1R,2E)-1-(acetyloxy)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-buten yl]-4-[(dimethylphenylsilyl)methyl]-2-phenyl-, (4R)-
Synonyms:
CAS NO:389807-13-0
Molecular Formula: C40H45NO5Si2
Molecular Weight: 675.972
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: 5(4H)-Oxazolone, 4-[(1R,2E)-1-(acetyloxy)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-buten yl]-4-[(dimethylphenylsilyl)methyl]-2-phenyl-, (4R)-(CAS DataBase Reference)
NIST Chemistry Reference: 5(4H)-Oxazolone, 4-[(1R,2E)-1-(acetyloxy)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-buten yl]-4-[(dimethylphenylsilyl)methyl]-2-phenyl-, (4R)-(389807-13-0)
EPA Substance Registry System: 5(4H)-Oxazolone, 4-[(1R,2E)-1-(acetyloxy)-4-[[(1,1-dimethylethyl)diphenylsilyl]oxy]-2-buten yl]-4-[(dimethylphenylsilyl)methyl]-2-phenyl-, (4R)-(389807-13-0)

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: 389807-13-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 389807-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,9,8,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 389807-13:
(8*3)+(7*8)+(6*9)+(5*8)+(4*0)+(3*7)+(2*1)+(1*3)=200
200 % 10 = 0
So 389807-13-0 is a valid CAS Registry Number.

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389807-13-0Relevant academic research and scientific papers

gem-diacetates as carbonyl surrogates for asymmetric synthesis. Total syntheses of sphingofungins E and F

Trost,Lee

, p. 12191 - 12201 (2007/10/03)

The equivalent of an asymmetric addition to a carbonyl group with a stabilized anion is accomplished by discriminating between the enantiotopic C-O single bonds of a gem-diacetate. In this way, enantioselective total syntheses of two antifugal agents, sph

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