Cas 109950-52-9,4-[1-Hydroxy-1-methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-3-methoxy-1-(4-methyl-pent-3-enyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester

109950-52-9

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Basic information

Product Name: 4-[1-Hydroxy-1-methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-3-methoxy-1-(4-methyl-pent-3-enyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester
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CAS NO:109950-52-9
Molecular Formula:
Molecular Weight: 408.535
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: 4-[1-Hydroxy-1-methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-3-methoxy-1-(4-methyl-pent-3-enyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[1-Hydroxy-1-methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-3-methoxy-1-(4-methyl-pent-3-enyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(109950-52-9)
EPA Substance Registry System: 4-[1-Hydroxy-1-methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-3-methoxy-1-(4-methyl-pent-3-enyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(109950-52-9)

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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 109950-52-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109950-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,5 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109950-52:
(8*1)+(7*0)+(6*9)+(5*9)+(4*5)+(3*0)+(2*5)+(1*2)=139
139 % 10 = 9
So 109950-52-9 is a valid CAS Registry Number.

109950-52-9Upstream product

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109950-52-9Relevant academic research and scientific papers

AN ALTERNATE SYNTHESIS OF FUROVENTALENE USING AN EXTENSION OF HAGIWARA'S CONSTRUCTION OF THE 3-METHYLFURAN MOIETY

Castanedo, Ricardo,Zetina, Carlos Bernardo,Maldonado, Luis Angel

, p. 175 - 178 (2007/10/02)

A new total synthesis of furoventalene 5 is reported.Key steps in the sequence are the Birch reduction-homoprenylation in situ of aromatic carboxylic acids precursors, construction of the 3-methylfuran moiety by Hagiwara's method and decarboxylative aroma

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