Cas 653591-57-2,(4R,5S)-3-{(2S,3R)-2-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one

653591-57-2

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Product Name: (4R,5S)-3-{(2S,3R)-2-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one
Synonyms: (4R,5S)-3-{(2S,3R)-2-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one
CAS NO:653591-57-2
Molecular Formula:
Molecular Weight: 607.819
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-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S)-3-{(2S,3R)-2-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one(653591-57-2)
EPA Substance Registry System: (4R,5S)-3-{(2S,3R)-2-[(2S,3S)-3-(tert-Butyl-dimethyl-silanyloxymethyl)-1,4-dioxa-spiro[4.5]dec-2-yl]-5-oxo-tetrahydro-furan-3-yl}-4,5-diphenyl-oxazolidin-2-one(653591-57-2)

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: 653591-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 653591-57-2 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, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 653591-57:
(8*6)+(7*5)+(6*3)+(5*5)+(4*9)+(3*1)+(2*5)+(1*7)=182
182 % 10 = 2
So 653591-57-2 is a valid CAS Registry Number.

653591-57-2Upstream product

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653591-57-2Relevant 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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