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Azuleno[6,5-b]furan-2,5-dione,3,3a,4,4a,7a,8,9,9a-octahydro-4-hydroxy-4a,8-dimethyl-3-methylene-,(3aS,4S,4aS,7aR,8R,9aR)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

110716-87-5

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110716-87-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 110716-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,7,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110716-87:
(8*1)+(7*1)+(6*0)+(5*7)+(4*1)+(3*6)+(2*8)+(1*7)=95
95 % 10 = 5
So 110716-87-5 is a valid CAS Registry Number.

110716-87-5Upstream product

110716-87-5Downstream Products

110716-87-5Relevant academic research and scientific papers

Helenanolides: Stereocontrolled Total Synthesis of dl-Bigelovin, dl-Mexicanin I, and dl-Linifolin A

Grieco, Paul A.,Ohfune, Yasufumi,Majetich, George F.

, p. 360 - 366 (2007/10/02)

Stereocontrolled total syntheses of the sesquiterpene lactones dl-bigelovin (11), dl-mexicanin I (12), and dl-linifolin A (13) are described.The syntheses start with the hydroazulenone 4 and proceed via the key epoxy alkohol 9.Elaboration of 9 into the tricyclic γ-lactone 14 dl-bigelovin. α-methylenation.Subsequent oxidation at C(4) completes the synthesis of dl-bigelovin.Epoxide opening of 9 with dilithioacetate provides access to tricyclic lactone 23 which gives way to 24 via reduction of ketone 25.Cleavage of the benzyl ether in 24 followed by α-methylenationand oxidation generates dl-mexicanin I.Acetylation of 12 affords dl-linifolin A.

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