28068-69-1 Usage
Molecular structure
Bicyclic, with two hydroxyl groups, three methyl groups, and a methylidene substituent.
Carbon atoms
15, as indicated by the name.
Oxygen atoms
Highly oxygenated, with at least two oxygen atoms in the hydroxyl groups and one in the ring structure.
Presence of a double bond
The compound has a double bond in its structure, which may affect its reactivity and properties.
Potential for biological activity
The complex structure and high oxygenation suggest that the compound may have potential biological applications.
Need for further research
The specific properties and potential applications of 2,12-dihydroxy-4,8,12-trimethyl-16-methylidene-14-oxabicyclo[11.3.1]heptadeca-4,8-dien-15-one are not yet known and require further investigation and analysis.
Check Digit Verification of cas no
The CAS Registry Mumber 28068-69-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,6 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28068-69:
(7*2)+(6*8)+(5*0)+(4*6)+(3*8)+(2*6)+(1*9)=131
131 % 10 = 1
So 28068-69-1 is a valid CAS Registry Number.
28068-69-1Relevant academic research and scientific papers
Synthesis of analogues of Eunicea γ-cembranolides containing cyclic ethers via saponification
Rodriguez,Pina,Acosta,Ramirez,Soto
, p. 648 - 658 (2007/10/03)
A method for the synthesis of derivatives of the lead structures euniolide (1), 12,13-bisepieupalmerin (2), and eupalmerin acetate (3) containing tetrahydrofuran and tetrahydropyran ring systems was developed on the basis of alkali-induced intramolecular oxacyclizations. Representatives of the new analogues were submitted to the in vitro antitumor cell-line-screening program of the National Cancer Institute (NCI). While it was shown that a variety of structural modifications are possible, these transformations led typically to nontoxic synthetic cembranoids.
Interconversion of Cembranolide &δ- and &γ-Lactones: Synthesis of the C-1 Epimer of Isolobophytolide
Marshall, James A.,Karas, Lawrence J.,Coghlan, Michael J.
, p. 699 - 701 (2007/10/02)
The δ-lactone cembranolide diterpene crassin alcohol (2) has been converted to an isomeric γ-lactone isocrassin alcohol (6) by a sequence involving kinetically controlled addition of benzenethiol to the conjugated lactone double bond followed by base-prom
