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1-Oxo-3-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester is a complex organic compound with the molecular formula C17H16O3. It is a derivative of naphthalene, a bicyclic aromatic hydrocarbon, and features a carboxylic acid group, an ester group, and a phenyl ring. 1-Oxo-3-phenyl-1,2,3,4-tetrahydro-naphthalene-2-carboxylic acid methyl ester is characterized by its unique structure, which includes a naphthalene core with a four-carbon chain attached to the second carbon, a carbonyl group at the first position, and a phenyl ring at the third position. The methyl ester group is attached to the carboxylic acid, making it a methyl ester derivative. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its versatile structure and reactivity. It is an intermediate in the production of certain drugs and can also be found in the composition of some fragrances and flavorings.

83303-54-2

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83303-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83303-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,3,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83303-54:
(7*8)+(6*3)+(5*3)+(4*0)+(3*3)+(2*5)+(1*4)=112
112 % 10 = 2
So 83303-54-2 is a valid CAS Registry Number.

83303-54-2Relevant academic research and scientific papers

Synthese de methoxycarbonylindenes, dihydro-1,2 naphtalenes et benzocycloheptene. Obtention des indanones-1, des tetralones-1 et de la benzosuberone correspondantes

Verbel, Joel,Carrie, Robert

, p. 116 - 124 (2007/10/02)

The synthesis of methoxycarbonylindenes, 1,2-dihydro-naphtalenes, and benzocycloheptene starting from the corresponding 1-indanones, 1-tetralones, and benzosuberone is reported.The starting ketones were synthesized by methods described in the literature which were optimized; in some cases new processes are described.

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