Cas 653591-63-0,(4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one

653591-63-0

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Basic information

Product Name: (4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one
Synonyms: (4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one
CAS NO:653591-63-0
Molecular Formula:
Molecular Weight: 593.676
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: (4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one(653591-63-0)
EPA Substance Registry System: (4R,5S)-3-[(2S,3R)-2-((1S,2S)-1,2-Bis-benzyloxy-3-hydroxy-propyl)-5-oxo-tetrahydro-furan-3-yl]-4,5-diphenyl-oxazolidin-2-one(653591-63-0)

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: 653591-63-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 653591-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,3,5,9 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 653591-63:
(8*6)+(7*5)+(6*3)+(5*5)+(4*9)+(3*1)+(2*6)+(1*3)=180
180 % 10 = 0
So 653591-63-0 is a valid CAS Registry Number.

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653591-63-0Relevant academic research and scientific papers

Synthesis of 1-Deoxy-D-galactohomonojirimycin via Enantiomerically Pure Allenylstannanes

Achmatowicz, Michal,Hegedus, Louis S.

, p. 2229 - 2234 (2007/10/03)

1-Deoxy-D-galactohomonojirimycin was synthesized in seven steps from optically pure allenylstannane 4 and L-lactate-derived aldehyde 5 in 48% overall yield. The key step was the Lewis acid catalyzed reaction of 4 and 5 to give the syn-amino alcohol in exc

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