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182426-37-5

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  • 3,8a,3',8'a-tetramethyl-5,5'-dimethylene-4,4a,5,6,7,8,8a,9,4',4'a,5',6',7',8',8'a,9'-hexadecahydro-[9a,9'a]bi[naphtho[2,3-b]furanyl]-2,2'-dione

    Cas No: 182426-37-5

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  • 3,8a,3',8'a-tetramethyl-5,5'-dimethylene-4,4a,5,6,7,8,8a,9,4',4'a,5',6',7',8',8'a,9'-hexadecahydro-[9a,9'a]bi[naphtho[2,3-b]furanyl]-2,2'-dione

    Cas No: 182426-37-5

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182426-37-5 Usage

General Description

The chemical "3,8a,3',8'a-tetramethyl-5,5'-dimethylene-4,4a,5,6,7,8,8a,9,4',4'a,5',6',7',8',8'a,9'-hexadecahydro-[9a,9'a]bi[naphtho[2,3-b]furanyl]-2,2'-dione" is a complex organic compound with a long and specific chemical structure. It is a dione derivative, containing multiple methyl groups and a fused bi[naphtho[2,3-b]furanyl] ring system. 3,8a,3',8'a-tetramethyl-5,5'-dimethylene-4,4a,5,6,7,8,8a,9,4',4'a,5',6',7',8',8'a,9'-hexadecahydro-[9a,9'a]bi[naphtho[2,3-b]furanyl]-2,2'-dione likely has a wide range of potential applications, including in pharmaceutical research, organic synthesis, and materials science, as its unique structure and properties could make it useful for various purposes. However, further research and testing would be necessary to fully understand and harness its potential.

Check Digit Verification of cas no

The CAS Registry Mumber 182426-37-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,4,2 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 182426-37:
(8*1)+(7*8)+(6*2)+(5*4)+(4*2)+(3*6)+(2*3)+(1*7)=135
135 % 10 = 5
So 182426-37-5 is a valid CAS Registry Number.

182426-37-5Downstream Products

182426-37-5Relevant articles and documents

Regioselectivity of dimerisation of butenolides via captodative stabilised radicaloid intermediates

Bagal, Sharanjeet K.,Adlington, Robert M.,Brown, Rohan A.B.,Baldwin, Jack E.

, p. 4633 - 4637 (2007/10/03)

The regioselective outcome observed during dimerisation of butenolides to dimeric structures via captodative stabilised radicaloids has been studied. The captodative stabilised radicaloids were generated by initial conversion of butenolides to chlorobutenolides via the corresponding hydroxybutenolides, followed by treatment with CoCl(PPh3)3.

Biomimetic synthesis of biatractylolide and biepiasterolide

Bagal, Sharanjeet K.,Adlington, Robert M.,Baldwin, Jack E.,Marquez, Rodolfo,Cowley, Andrew

, p. 3049 - 3052 (2007/10/03)

(Matrix presented) The biomimetic synthesis of the bisesquiterpenoids biatractylolide 1 and biepiasterolide 2 is reported.

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