Cas 227097-96-3,2-Propenoic acid, 3-[3,4-bis(acetyloxy)phenyl]-, 1-(methoxycarbonyl)-1,2-ethanediyl ester, (2E,2'E)-

227097-96-3

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Basic information

Product Name: 2-Propenoic acid, 3-[3,4-bis(acetyloxy)phenyl]-, 1-(methoxycarbonyl)-1,2-ethanediyl ester, (2E,2'E)-
Synonyms:
CAS NO:227097-96-3
Molecular Formula: C30H28O14
Molecular Weight: 612.544
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-[3,4-bis(acetyloxy)phenyl]-, 1-(methoxycarbonyl)-1,2-ethanediyl ester, (2E,2'E)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Propenoic acid, 3-[3,4-bis(acetyloxy)phenyl]-, 1-(methoxycarbonyl)-1,2-ethanediyl ester, (2E,2'E)-(227097-96-3)
EPA Substance Registry System: 2-Propenoic acid, 3-[3,4-bis(acetyloxy)phenyl]-, 1-(methoxycarbonyl)-1,2-ethanediyl ester, (2E,2'E)-(227097-96-3)

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: 227097-96-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 227097-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,0,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 227097-96:
(8*2)+(7*2)+(6*7)+(5*0)+(4*9)+(3*7)+(2*9)+(1*6)=153
153 % 10 = 3
So 227097-96-3 is a valid CAS Registry Number.

227097-96-3Upstream product

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227097-96-3Relevant academic research and scientific papers

Chicoric acid analogues as HIV-1 integrase inhibitors

Lin, Zhaiwei,Neamati, Nouri,Zhao, He,Kiryu, Yoshimitsu,Turpin, Jim A.,Aberham, Claudia,Strebel, Klaus,Kohn, Kurt,Witvrouw, Myriam,Pannecouque, Christophe,Debyser, Zeger,De Clercq, Erik,Rice, William G.,Pommier, Yves,Burke Jr., Terrence R.

, p. 1401 - 1414 (1999)

The present study was undertaken to examine structural features of L- chicoric acid (3) which are important for potency against purified HIV-1 integrase and for reported cytoprotective effects in cell-based systems. Through a progressive series of analogu

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