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Ethyl 2-(4-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate is a complex organic compound with the chemical formula C14H14O3. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a ketone group at the 4-position and an ester group at the 2-position. ethyl 2-(4-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)acetate is characterized by its molecular structure, which includes a saturated ring (tetrahydronaphthalene) fused to an aromatic ring, with an ethyl ester group attached to the 2-position of the aromatic ring. It is an intermediate in the synthesis of various pharmaceuticals and chemical compounds, and its properties, such as solubility and reactivity, are influenced by its molecular structure.

5386-94-7

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5386-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5386-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,8 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5386-94:
(6*5)+(5*3)+(4*8)+(3*6)+(2*9)+(1*4)=117
117 % 10 = 7
So 5386-94-7 is a valid CAS Registry Number.

5386-94-7Upstream product

5386-94-7Relevant academic research and scientific papers

Enantioselective synthesis of 2,6-cis-disubstituted tetrahydropyrans via a tandem catalytic asymmetric hydrogenation/oxa-Michael cyclization: An efficient approach to (-)-centrolobine

Xie, Jian-Hua,Guo, Lu-Chuan,Yang, Xiao-Hui,Wang, Li-Xin,Zhou, Qi-Lin

supporting information, p. 4758 - 4761,4 (2012/12/13)

A highly efficient one-pot process via a tandem reaction of catalytic asymmetric hydrogenation and oxa-Michael cyclization for the synthesis of 2,6-cis-disubstituted tetrahydropyrans has been developed (ee up to 99.9%, cis/trans-selectivity up to 99:1). T

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