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(1S)-1,2,3,4,4a,9,10,10aα-Octahydro-1α,4aβ-dimethylphenanthrene-1β-methanol is a complex organic compound belonging to the class of phenanthrenes, which are tricyclic aromatic hydrocarbons. This specific compound is characterized by its octahydro structure, meaning it contains eight hydrogen atoms bonded to carbon atoms in a cyclic manner. The presence of two methyl groups at the 1α and 4aβ positions, along with a hydroxyl group (-OH) at the 1β position, further defines its unique chemical structure. This molecule is a chiral compound, indicated by the "1S" prefix, which denotes the specific arrangement of atoms in three-dimensional space. The compound's structure and properties make it a potential candidate for various applications in the fields of chemistry and materials science, such as in the synthesis of pharmaceuticals or as a precursor in the production of other organic compounds.

727-20-8

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727-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 727-20-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,2 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 727-20:
(5*7)+(4*2)+(3*7)+(2*2)+(1*0)=68
68 % 10 = 8
So 727-20-8 is a valid CAS Registry Number.

727-20-8Relevant academic research and scientific papers

Organoiron complexes of podocarpic acid derivatives

Cambie, Richard C.,Metzler, Michael R.,Rutledge, Peter S.,Woodgate, Paul D.

, p. 117 - 131 (2007/10/02)

Treatment of the non-conjugated 1,4-dienes obtained by Birch reduction of podocarpa-8,11,13-trien-19-ol (2) and 12,19-dimethoxypodocarpa-8,11,13-triene (4) with Fe3(CO)12 leads (albeit in low yields) in each case to a mixture of η4-1,3-diene iron complexes whose structure have been assigned by NMR spectroscopy.One of these complexes has been successfully converted into a cationic η5-dienyl iron salt (35) by treatment with acid.Attempted complexation of the 1,4-dienol ethers by treatment with a variety of sources of Fe(CO)3 under mild conditions has led to the conclusion that prior conversion of a 1,4-dienol ether into a 1,3-dienol ether is necessary for success.In model studies, treatment of 1-methoxy-3,4-dimethylcyclohexa-1,4-diene (9) with Fe3(CO)12 has given η4-diene and subsequently η5-dienyl iron complexes.

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