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Ethyl 3-chlorophenyl carbonate is an organic compound with the chemical formula C9H9ClO3. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 200.61 g/mol. ethyl 3-chlorophenyl carbonate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is synthesized through the reaction of 3-chlorophenol with ethyl chloroformate, a process that involves the formation of a carbonate ester. Ethyl 3-chlorophenyl carbonate is known for its reactivity and is often used in the preparation of biologically active compounds due to its ability to undergo nucleophilic substitution reactions. It is important to handle ethyl 3-chlorophenyl carbonate with care due to its potential toxicity and reactivity.

1847-87-6

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1847-87-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1847-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1847-87:
(6*1)+(5*8)+(4*4)+(3*7)+(2*8)+(1*7)=106
106 % 10 = 6
So 1847-87-6 is a valid CAS Registry Number.

1847-87-6Relevant academic research and scientific papers

A new, mild, general and efficient route to aryl ethyl carbonates in solvent-free conditions promoted by magnesium perchlorate

Bartoli, Giuseppe,Bosco, Marcella,Carlone, Armando,Locatelli, Manuela,Marcantoni, Enrico,Melchiorre, Paolo,Palazzi, Paolo,Sambri, Letizia

, p. 4429 - 4434 (2006)

A new, general and mild method for the direct synthesis of aryl and alkyl ethyl carbonates promoted by a Lewis acid is reported. The reaction proceeds smoothly with diethyl dicarbonate in the presence of Mg(ClO4) 2, a specific activator of 1,3-dicarbonyl compounds, and shows general applicability. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

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