Cas 862469-20-3,ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate

862469-20-3

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Basic information

Product Name: ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate
Synonyms: ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate
CAS NO:862469-20-3
Molecular Formula:
Molecular Weight: 294.348
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: ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate(862469-20-3)
EPA Substance Registry System: ethyl (2E)-3-[5-methoxy-2-(methoxymethoxy)-4-methylphenyl]but-2-enoate(862469-20-3)

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: 862469-20-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862469-20-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,6 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 862469-20:
(8*8)+(7*6)+(6*2)+(5*4)+(4*6)+(3*9)+(2*2)+(1*0)=193
193 % 10 = 3
So 862469-20-3 is a valid CAS Registry Number.

862469-20-3Upstream product

867-13-0 diethoxyphosphoryl-acetic acid ethyl ester

862469-20-3Downstream Products

862469-20-3Relevant academic research and scientific papers

Strategies for the total asymmetric synthesis of heliannuols K and L: Scope and limitations

Lecornue, Frederic,Paugam, Renee,Ollivier, Jean

, p. 2589 - 2598 (2005)

Kulinkovich reactions of oxa-esters bearing terminal double bonds afford cyclopropanols by intramolecular cyclization. These can undergo Saegusa oxidation to provide β-chlorooxacycloalkanones and can then be then dehydrohalogenated into oxacycloalkenones.

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