Cas 863891-54-7,(4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one

863891-54-7

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Basic information

Product Name: (4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one
Synonyms: (4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one
CAS NO:863891-54-7
Molecular Formula:
Molecular Weight: 515.725
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: (4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one(863891-54-7)
EPA Substance Registry System: (4S)-3-[1-hexyl-4-oxo-3-phenyl-5-trimethylsilylbicyclo[3.1.0]-2-hexene-6(R)-oyl]-4-phenyloxazolidin-2-one(863891-54-7)

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: 863891-54-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 863891-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,3,8,9 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 863891-54:
(8*8)+(7*6)+(6*3)+(5*8)+(4*9)+(3*1)+(2*5)+(1*4)=217
217 % 10 = 7
So 863891-54-7 is a valid CAS Registry Number.

863891-54-7Upstream product

678195-55-6 (R)-3-((R)-2-Hexyl-cycloprop-2-enecarbonyl)-4-phenyl-oxazolidin-2-one

863891-54-7Downstream Products

863891-54-7Relevant academic research and scientific papers

Diastereoselective intermolecular Pauson-Khand reactions of chiral cyclopropenes

Pallerla, Mahesh K.,Fox, Joseph M.

, p. 3593 - 3595 (2005)

(Chemical Equation Presented) In this Letter, it is demonstrated that the unusual reactivity of cyclopropenes can increase the scope and utility of intermolecular Pauson-Khand reactions. The well-defined chiral environment of cyclopropenes has a powerful

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