Cas 85873-06-9,(6E,10E)-8-Hydroxy-12-(2-hydroxy-5-methoxy-3-methyl-phenyl)-2,6,10-trimethyl-dodeca-6,10-dienoic acid methyl ester

85873-06-9

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Basic information

Product Name: (6E,10E)-8-Hydroxy-12-(2-hydroxy-5-methoxy-3-methyl-phenyl)-2,6,10-trimethyl-dodeca-6,10-dienoic acid methyl ester
Synonyms:
CAS NO:85873-06-9
Molecular Formula:
Molecular Weight: 404.547
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: (6E,10E)-8-Hydroxy-12-(2-hydroxy-5-methoxy-3-methyl-phenyl)-2,6,10-trimethyl-dodeca-6,10-dienoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (6E,10E)-8-Hydroxy-12-(2-hydroxy-5-methoxy-3-methyl-phenyl)-2,6,10-trimethyl-dodeca-6,10-dienoic acid methyl ester(85873-06-9)
EPA Substance Registry System: (6E,10E)-8-Hydroxy-12-(2-hydroxy-5-methoxy-3-methyl-phenyl)-2,6,10-trimethyl-dodeca-6,10-dienoic acid methyl ester(85873-06-9)

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: 85873-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85873-06-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,7 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85873-06:
(7*8)+(6*5)+(5*8)+(4*7)+(3*3)+(2*0)+(1*6)=169
169 % 10 = 9
So 85873-06-9 is a valid CAS Registry Number.

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85873-06-9Relevant academic research and scientific papers

DITERPENOID METABOLITES FROM THE MARINE ALGA CYSTOSEIRA ELEGANS

Banaigs, B.,Francisco, C.,Gonzalez, E.,Fenical, William

, p. 629 - 638 (1983)

The isolation and structure determination of three new diterpenoids from the brown alga Cystoseira elegans is reported.The structures of these compounds were determined by combined chemical and spectral (13C and 1H NMR with decoupling experiments, high re

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