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3a(1H)-Pentalenecarboxylic acid, 2,3,6,6a-tetrahydro-4-methyl-3-oxo-, methyl ester, (3aR,6aS)-rel-(9CI) is a complex organic compound with the molecular formula C12H16O3. It is a derivative of pentalene, a polycyclic aromatic hydrocarbon, and features a carboxylic acid group that has been esterified with methanol to form a methyl ester. The compound has a unique stereochemistry, with the (3aR,6aS)-rel configuration indicating the specific arrangement of atoms in three-dimensional space. This molecule is of interest in organic chemistry and may have potential applications in the synthesis of more complex molecules or as a precursor in pharmaceutical or materials science research.

811784-61-9

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811784-61-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 811784-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,1,7,8 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 811784-61:
(8*8)+(7*1)+(6*1)+(5*7)+(4*8)+(3*4)+(2*6)+(1*1)=169
169 % 10 = 9
So 811784-61-9 is a valid CAS Registry Number.

811784-61-9Upstream product

811784-61-9Downstream Products

811784-61-9Relevant academic research and scientific papers

Development of palladium(II)-catalyzed oxidative cyclization of olefinic keto and/or lactone esters

Hibi, Ayaka,Toyota, Masahiro

scheme or table, p. 4888 - 4891 (2009/12/01)

A highly efficient palladium-catalyzed oxidative cyclization of olefinic keto and/or lactone esters, which features a catalytic cyclization employing one atmosphere of oxygen as a reoxidizing agent, is developed.

Gold(I)-catalyzed 5-endo-dig carbocyclization of acetylenic dicarbonyl compounds

Staben, Steven T.,Kennedy-Smith, Joshua J.,Toste, F. Dean

, p. 5350 - 5352 (2007/10/03)

Cyclopentenoid structures including compounds containing vinyl iodide, 1,3-diene, and heterocyclic moieties are obtained through the gold(I)-catalyzed 5-endo-dig addition of β-dicarbonyl compounds to unactivated alkynes under neutral conditions and at room temperature (RT). Both monocyclic and bicyclic cyclopentenes can be formed in excellent yields and with good diastereoselectivity (see scheme).

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