Cas 1244612-52-9,ethyl [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate

1244612-52-9

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Basic information

Product Name: ethyl [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate
Synonyms: ethyl [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate
CAS NO:1244612-52-9
Molecular Formula:
Molecular Weight: 372.505
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 [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate(1244612-52-9)
EPA Substance Registry System: ethyl [2-(2-methoxy-4-methylphenyl)carbonyl]-5-methyl-2-(3-methylbut-2-en-1-yl)hex-4-enoatehex-4-enoate(1244612-52-9)

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: 1244612-52-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1244612-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,4,6,1 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1244612-52:
(9*1)+(8*2)+(7*4)+(6*4)+(5*6)+(4*1)+(3*2)+(2*5)+(1*2)=129
129 % 10 = 9
So 1244612-52-9 is a valid CAS Registry Number.

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1244612-52-9Relevant academic research and scientific papers

Efficient total synthesis of racemic bisabolane sesquiterpenes curcuphenol and xanthorrhizol starting from substituted acetophenones

Montiel, Luisa E.,Zepeda, L. Gerardo,Tamariz, Joaquin

scheme or table, p. 1261 - 1273 (2010/09/07)

A total synthesis of natural bisabolane sesquiterpenes curcuphenol (1) and xanthorrhizol (2) was developed by using the substituted acetophenones 4 and 5, respectively, as starting materials. The acetyl group of the latter was activated through ethoxycarb

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