Cas 946572-74-3,8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester

946572-74-3

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Basic information

Product Name: 8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester
Synonyms: 8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester
CAS NO:946572-74-3
Molecular Formula:
Molecular Weight: 334.456
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: 8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester(946572-74-3)
EPA Substance Registry System: 8-methlnonanoic acid (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propen-1-yl ester(946572-74-3)

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: 946572-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 946572-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,5,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 946572-74:
(8*9)+(7*4)+(6*6)+(5*5)+(4*7)+(3*2)+(2*7)+(1*4)=213
213 % 10 = 3
So 946572-74-3 is a valid CAS Registry Number.

946572-74-3Upstream product

946572-74-3Downstream Products

946572-74-3Relevant academic research and scientific papers

Isolation of coniferyl esters from Capsicum baccatum L., and their enzymatic preparation and agonist activity for TRPV1

Kobata, Kenji,Tate, Hitomi,Iwasaki, Yusaku,Tanaka, Yoshiyuki,Ohtsu, Keigo,Yazawa, Susumu,Watanabe, Tatsuo

, p. 1179 - 1184 (2008)

Coniferyl esters-capsiconiate and dihydrocapsiconiate-were isolated from the fruits of the pepper, Capsicum baccatum L. var. praetermissum. Their structures were determined by spectroscopic methods to be coniferyl (E)-8-methyl-6-nonenoate (capsiconiate) a

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