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2-Chlor-benzoyl-malonsaeure-diethylester, also known as 2-chlorobenzoyl malonic acid diethyl ester, is an organic compound with the chemical formula C12H12Cl2O4. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. 2-Chlor-benzoyl-malonsaeure-diethylester is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. It is derived from the reaction of 2-chlorobenzoyl chloride with diethyl malonate, and its chemical structure features a 2-chlorobenzoyl group attached to a malonic acid diethyl ester moiety. Due to its reactivity and potential applications, 2-chlorobenzoyl malonic acid diethyl ester is an important compound in the field of organic chemistry and chemical synthesis.

3516-73-2

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3516-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3516-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3516-73:
(6*3)+(5*5)+(4*1)+(3*6)+(2*7)+(1*3)=82
82 % 10 = 2
So 3516-73-2 is a valid CAS Registry Number.

3516-73-2Relevant academic research and scientific papers

Zinc-mediated alkylation and acylation of 1,3-dicarbonyl compounds

Yadav,Reddy, B. V. Subba,Mishra, Anand Kumar

, p. 280 - 281 (2010)

1,3-Dicarbonyl compounds undergo smooth allylation, benzylation, propargylation, and acylation with halides using metallic zinc in DMF at 60 °C to afford the corresponding allyl, benzyl, 2-propynyl, and acylated 1,3-diesters in good yields. In the case of cyclic 1,3-diketones, the corresponding enol ethers are obtained as sole products instead of C-alkylation.

Cycloaracylation of Enamines, I. - Synthesis of 4-Quinolone-3-carboxylic Acids

Grohe, Klaus,Heitzer, Helmut

, p. 29 - 37 (2007/10/02)

Starting with o-halobenzoyl chlorides 4 and open-chain secondary enamines 5, a new synthesis of 4-quinolone-3-carboxylic acids 12 is described.The reaction of 7-haloquinolone-3-carboxylic acids 12a-k with aliphatic amines 14 produces highly active antibacterial 7-aminoquinolone-3-carboxylic acids 15.The main product of the 1-cyclopropyl series, "ciprofloxacin" (15a), is being developed as a broad-spectrum chemotherapeutic agent.

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