Product Name:Methyl 2-Chloro-D-mandelate
IUPAC Name:methyl (2S)-2-(2-chlorophenyl)-2-hydroxyacetate
| Packing Unit | Available Stock | Price($) | Quantity |
|---|---|---|---|
| CM395726-25g | in stock | ȃŤ |
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| CM395726-100g | in stock | ǙȃǙ |
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| Product Overview |
Methyl 2-Chloro-D-mandelate is an organic compound that has been studied for its potential applications in the fields of medicine, biochemistry, and physiology. It is a derivative of the widely used pharmaceutical drug chlorpheniramine, and has been found to have a variety of biological effects on the body. |
| Synthesis and Application |
Methyl 2-Chloro-D-mandelate is synthesized from chlorpheniramine through a series of chemical reactions. The first step is the conversion of chlorpheniramine to its 2-chloro-2-hydroxyacetyl derivative, which is achieved by the reaction of chlorpheniramine with 2-chloro-2-hydroxyacetic acid in the presence of an acid catalyst. The next step is the methylation of the 2-chloro-2-hydroxyacetyl derivative to form Methyl 2-Chloro-D-mandelate. This is accomplished by reacting the 2-chloro-2-hydroxyacetyl derivative with dimethyl sulfate in the presence of a base catalyst. Methyl 2-Chloro-D-mandelate has been studied for its potential applications in the fields of medicine, biochemistry, and physiology. In the medical field, it has been studied for its potential as an anti-inflammatory, anti-allergenic, and anti-histamine agent. In the field of biochemistry, it has been studied for its potential to inhibit the release of histamine from mast cells, and in the field of physiology, it has been studied for its potential to modulate the activity of the autonomic nervous system. |
| Future Directions |
There are several potential future directions for research on Methyl 2-Chloro-D-mandelate. One potential direction is to further investigate the potential anti-inflammatory, anti-allergenic, and anti-histamine effects of this compound. Additionally, further research could be done to explore the potential of this compound to modulate the activity of the autonomic nervous system. Finally, further research could be done to explore the potential of this compound to inhibit the enzyme histamine N-methyltransferase. |
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