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Ethyl 2-amino-2-methylpropanoate p-toluenesulfonic acid salt is a chemical compound that can be described as a derivative of the amino acid leucine, with an ethyl ester group attached to the carboxylic acid moiety and a p-toluenesulfonic acid salt group as a counterion. ethyl 2-amino-2-methylpropanoate p-toluenesulfonic acid salt is synthesized by the reaction of ethyl 2-amino-2-methylpropanoate with p-toluenesulfonic acid, resulting in the formation of an ionic salt. It is a white crystalline solid and is soluble in water and organic solvents. The compound has potential applications in pharmaceuticals, as a building block for the synthesis of more complex molecules, and in the study of amino acid derivatives. Its chemical structure and properties make it a versatile intermediate in organic synthesis and a subject of interest in chemical research.

4783-14-6

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4783-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4783-14-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,8 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4783-14:
(6*4)+(5*7)+(4*8)+(3*3)+(2*1)+(1*4)=106
106 % 10 = 6
So 4783-14-6 is a valid CAS Registry Number.

4783-14-6Downstream Products

4783-14-6Relevant academic research and scientific papers

Dihydro-1,2,4-triazin-6(1H)-ones. II synthesis of several methylated 3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-ones

Collins, David J.,Hughes, Timothy C.,Johnson, Wynona M.

, p. 379 - 385 (1999)

Novel syntheses of 4,5-dihydro-1,2,4-triazin-6(1H)-ones were developed by use of imidoyl chlorides. The overall yield of 4,5-dihydro-1,2,4-triazin-6(1H)-ones prepared from amino acid imidates and hydrazines was improved by the development of a much more efficient synthesis of the imidates. The new 1,2-, 1,4- and 5,5-dimethyl dihydro-1,2,4-triazin-6(1H)-ones have been synthesized by cyclocondensation/cycloaddition pathways. Base-catalysed methylation of 3-phenyl-4,5-dihydro-1,2,4-triazin-6(1H)-one (15) gave the 1-methylated derivative (8); under similar conditions 2-methyl-3-phenyl-2,5-dihydro-1,2,4-triazin-6(1H)-one (9) afforded the 1,2-dimethyl derivative (7).

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