Cas 1062291-87-5,methyl (2S,3R)-3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-{[methoxy(methyl)amino]carbonyl}pent-4-enoate

1062291-87-5

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Basic information

Product Name: methyl (2S,3R)-3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-{[methoxy(methyl)amino]carbonyl}pent-4-enoate
Synonyms:
CAS NO:1062291-87-5
Molecular Formula:
Molecular Weight: 469.653
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: methyl (2S,3R)-3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-{[methoxy(methyl)amino]carbonyl}pent-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (2S,3R)-3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-{[methoxy(methyl)amino]carbonyl}pent-4-enoate(1062291-87-5)
EPA Substance Registry System: methyl (2S,3R)-3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-2-{[methoxy(methyl)amino]carbonyl}pent-4-enoate(1062291-87-5)

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: 1062291-87-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1062291-87-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,2,2,9 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1062291-87:
(9*1)+(8*0)+(7*6)+(6*2)+(5*2)+(4*9)+(3*1)+(2*8)+(1*7)=135
135 % 10 = 5
So 1062291-87-5 is a valid CAS Registry Number.

1062291-87-5Upstream product

791602-99-8 (2E)-4-(tert-butyldiphenylsiloxy)-but-2-enyl methyl carbonate

1062291-87-5Downstream Products

1062291-87-5Relevant academic research and scientific papers

Preparation of 2,4-disubstituted cyclopentenones by enantioselective iridium-catalyzed allylic alkylation: Synthesis of 2′-methylcarbovir and TEI-9826

Duebon, Pierre,Schelwies, Mathias,Helmchen, Guenter

, p. 6722 - 6733 (2008)

A broadly applicable synthesis of chiral 2- or 2,4-substituted cyclopent-2-enones has been developed by combining asymmetric iridium-catalyzed allylic alkylation reactions and ruthenium-catalyzed ring-closing meta-thesis. Enantiomeric excesses (ee values)

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