Cas 1443224-00-7,(2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate

1443224-00-7

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Basic information

Product Name: (2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate
Synonyms: (2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate
CAS NO:1443224-00-7
Molecular Formula:
Molecular Weight: 453.579
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: (2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate(CAS DataBase Reference)
NIST Chemistry Reference: (2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate(1443224-00-7)
EPA Substance Registry System: (2E,4Z)-methyl 6-((4E,6E)-N-(4-methoxybenzyl)-6,8-dimethyl-3-oxonona-4,6-dienamido)-5-methylhexa-2,4-dienoate(1443224-00-7)

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: 1443224-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1443224-00-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,2,2 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1443224-00:
(9*1)+(8*4)+(7*4)+(6*3)+(5*2)+(4*2)+(3*4)+(2*0)+(1*0)=117
117 % 10 = 7
So 1443224-00-7 is a valid CAS Registry Number.

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1443224-00-7Relevant academic research and scientific papers

An efficient synthesis of the fully elaborated isoindolinone unit of muironolide A

Xiao, Qing,Young, Kyle,Zakarian, Armen

, p. 3314 - 3317 (2013/07/26)

An efficient stereocontrolled construction of the fully substituted isoindolone subunit of muironolide A is described. The approach is centered on the intramolecular Diels-Alder reaction between the enol form of the β-keto amide and an α,β,γ,δ-unsaturated ester, followed by the installation of the cyclohexene double bond.

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