Cas 220284-22-0,selenocarbonic acid O-[5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-pent-3-ynyl] ester Se-phenyl ester

220284-22-0

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Basic information

Product Name: selenocarbonic acid O-[5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-pent-3-ynyl] ester Se-phenyl ester
Synonyms:
CAS NO:220284-22-0
Molecular Formula:
Molecular Weight: 411.475
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: selenocarbonic acid O-[5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-pent-3-ynyl] ester Se-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: selenocarbonic acid O-[5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-pent-3-ynyl] ester Se-phenyl ester(220284-22-0)
EPA Substance Registry System: selenocarbonic acid O-[5-(tert-butyl-dimethyl-silanyloxy)-1-methyl-pent-3-ynyl] ester Se-phenyl ester(220284-22-0)

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: 220284-22-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220284-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,2,8 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 220284-22:
(8*2)+(7*2)+(6*0)+(5*2)+(4*8)+(3*4)+(2*2)+(1*2)=90
90 % 10 = 0
So 220284-22-0 is a valid CAS Registry Number.

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220284-22-0Relevant academic research and scientific papers

Enantioselective synthesis of the 4-hydroxy buteneolide terminus of mucocin and related annonaceous acetogenins

Evans, P. Andrew,Murthy, V. Srinivasa

, p. 9627 - 9628 (1998)

The 4-hydroxy buteneolide terminus 3, applicable to mucocin 1 and related annonaceous acetogenins, was prepared in an expeditious manner from the selenocarbonate 2 via an intramolecular acyl radical cyclization followed by an enantioselective Lewis-acid catalyzed Keck-allylation reaction.

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