Cas 220784-92-9,(R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one

220784-92-9

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Basic information

Product Name: (R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one
Synonyms: (R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one
CAS NO:220784-92-9
Molecular Formula:
Molecular Weight: 377.556
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: (R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one(220784-92-9)
EPA Substance Registry System: (R)-3-Benzyl-4-[(Z)-(S)-4-(tert-butyl-dimethyl-silanyloxy)-1-hydroxy-but-2-enyl]-oxazolidin-2-one(220784-92-9)

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: 220784-92-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220784-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,7,8 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220784-92:
(8*2)+(7*2)+(6*0)+(5*7)+(4*8)+(3*4)+(2*9)+(1*2)=129
129 % 10 = 9
So 220784-92-9 is a valid CAS Registry Number.

220784-92-9Upstream product

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220784-92-9Relevant academic research and scientific papers

New entry for asymmetric deoxyazasugar synthesis: Syntheses of deoxymannojirimycin, deoxyaltrojirimycin and deoxygalactostatin

Asano, Koji,Hakogi, Toshikazu,Iwama, Seiji,Katsumura, Shigeo

, p. 41 - 42 (1999)

Deoxyazasugars such as deoxymannojirimycin, deoxyaltrojirimycin and deoxygalactostatin were stereoselectively synthesized starting from (R)-(+)-4-methoxycarbonyloxazolidinoe via a bicyclic oxazolidinylpiperidine as a common synthetic intermediate.

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