
CAS 177785-14-7
:methyl 2-(chloromethyl)nicotinate
Description:
Methyl 2-(chloromethyl)nicotinate is a chemical compound that belongs to the class of nicotinic acid derivatives. It features a methyl ester functional group and a chloromethyl substituent on the pyridine ring, which contributes to its reactivity and potential applications in organic synthesis. The presence of the chloromethyl group makes it a useful intermediate for further chemical transformations, such as nucleophilic substitution reactions. This compound is typically a solid at room temperature and is soluble in organic solvents, which facilitates its use in various chemical reactions. Methyl 2-(chloromethyl)nicotinate may exhibit biological activity, making it of interest in medicinal chemistry for the development of pharmaceuticals. As with many chlorinated compounds, it is important to handle it with care due to potential toxicity and environmental concerns. Proper safety measures should be observed when working with this substance in laboratory settings.
- 2-Chloromethyl-nicotinic acid methyl ester
- methyl 2-(chloromethyl)pyridine-3-carboxylate
- 3-Pyridinecarboxylic acid, 2-(chloromethyl)-, methyl ester
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Found 4 products.
3-Pyridinecarboxylic acid, 2-(chloromethyl)-, methyl ester
CAS:Formula:C8H8ClNO2Purity:95%Color and Shape:SolidMolecular weight:185.6076Methyl 2-(chloromethyl)nicotinate
CAS:Methyl 2-(chloromethyl)nicotinatePurity:95%Molecular weight:185.61g/molMETHYL 2-(CHLOROMETHYL)NICOTINATE
CAS:Formula:C8H8ClNO2Purity:95%Color and Shape:SolidMolecular weight:185.61Methyl 2-(chloromethyl)nicotinate
CAS:<p>Methyl 2-(chloromethyl)nicotinate is an organic compound that belongs to the class of esters. It is a reaction product of methyl 3-hydroxybenzoate and nitrous acid. This compound has antimicrobial activity and can be used to treat bacterial infections. Methyl 2-(chloromethyl)nicotinate has been shown to inhibit the growth of various bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Salmonella typhi, and Salmonella typhimurium. The cyano group in this molecule may be responsible for its antibacterial activity. <br>The efficiency of methyl 2-(chloromethyl)nicotinate varies with different types of bacteria. For example, it was more effective against MRSA than against Escherichia coli or Klebsiella pneumoniae</p>Formula:C8H8ClNO2Purity:Min. 95%Molecular weight:185.61 g/mol



