Cas 791096-70-3,2-Propenoic acid, 3-(1,4-dimethoxy-3-methyl-2-naphthalenyl)-3-(4-methoxyphenyl)-, ethyl ester, (2Z)-

791096-70-3

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Basic information

Product Name: 2-Propenoic acid, 3-(1,4-dimethoxy-3-methyl-2-naphthalenyl)-3-(4-methoxyphenyl)-, ethyl ester, (2Z)-
Synonyms:
CAS NO:791096-70-3
Molecular Formula: C25H26O5
Molecular Weight: 406.478
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: 2-Propenoic acid, 3-(1,4-dimethoxy-3-methyl-2-naphthalenyl)-3-(4-methoxyphenyl)-, ethyl ester, (2Z)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propenoic acid, 3-(1,4-dimethoxy-3-methyl-2-naphthalenyl)-3-(4-methoxyphenyl)-, ethyl ester, (2Z)-(791096-70-3)
EPA Substance Registry System: 2-Propenoic acid, 3-(1,4-dimethoxy-3-methyl-2-naphthalenyl)-3-(4-methoxyphenyl)-, ethyl ester, (2Z)-(791096-70-3)

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: 791096-70-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 791096-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,0,9 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 791096-70:
(8*7)+(7*9)+(6*1)+(5*0)+(4*9)+(3*6)+(2*7)+(1*0)=193
193 % 10 = 3
So 791096-70-3 is a valid CAS Registry Number.

791096-70-3Upstream product

791096-70-3Downstream Products

840503-70-0 (Z)-3-(1,4-Dimethoxy-3-methyl-naphthalen-2-yl)-3-(4-methoxy-phenyl)-acrylic acid

791096-70-3Relevant academic research and scientific papers

Asymmetric synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6-(4- hydroxyphenyl)hexanoic acid as a key intermediate for a neurodegenerative disease agent

Ikemoto, Tomomi,Nagata, Toshiaki,Yamano, Mitsuhisa,Ito, Tatsuya,Mizuno, Yukio,Tomimatsu, Kiminori

, p. 7757 - 7760 (2007/10/03)

An asymmetric synthesis of (R)-(+)-6-(1,4-dimethoxy-3-methyl-2-naphthyl)-6- (4-hydroxyphenyl)hexanoic acid 2 as a key intermediate for a neurodegenerative disease agent 1 has been developed. A key reaction was an asymmetric hydrogenation of hindered acryl

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