Cas 1062292-58-3,methyl (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate

1062292-58-3

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Basic information

Product Name: methyl (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate
Synonyms: methyl (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate
CAS NO:1062292-58-3
Molecular Formula:
Molecular Weight: 277.32
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 (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate(1062292-58-3)
EPA Substance Registry System: methyl (4E)-2-{[methoxy(methyl)amino]carbonyl}-5-phenylpent-4-enoate(1062292-58-3)

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: 1062292-58-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1062292-58-3 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 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1062292-58:
(9*1)+(8*0)+(7*6)+(6*2)+(5*2)+(4*9)+(3*2)+(2*5)+(1*8)=133
133 % 10 = 3
So 1062292-58-3 is a valid CAS Registry Number.

1062292-58-3Upstream product

87802-71-9 (E)-methyl cinnamyl carbonate

1062292-58-3Downstream Products

1062292-58-3Relevant 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

experimental part, p. 6722 - 6733 (2009/09/05)

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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