Cas 906450-06-4,methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate

906450-06-4

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Basic information

Product Name: methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate
Synonyms: methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate
CAS NO:906450-06-4
Molecular Formula:
Molecular Weight: 316.397
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: methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate(906450-06-4)
EPA Substance Registry System: methyl 2-methoxy-1-(2'-(3''-methoxyphenyl)ethyl)-5-methylcyclohexa-2,5-diene-1-carboxylate(906450-06-4)

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: 906450-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 906450-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,4,5 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 906450-06:
(8*9)+(7*0)+(6*6)+(5*4)+(4*5)+(3*0)+(2*0)+(1*6)=154
154 % 10 = 4
So 906450-06-4 is a valid CAS Registry Number.

906450-06-4Upstream product

906450-06-4Downstream Products

906450-06-4Relevant academic research and scientific papers

A formal total synthesis of the marine diterpenoid diisocyanoadociane

Fairweather, Kelly A.,Mander, Lewis N.

, p. 3395 - 3398 (2006)

A formal total synthesis of diisocyanoadociane, a marine diterpenoid with potent antimalarial properties, has been completed. The synthesis begins with a phenanthrenoid precursor that is transformed into a pyrene-derived intermediate by means of an intram

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