CAS 36340-61-1
:4-chloro-6-methylpyridin-2-amine
Description:
4-Chloro-6-methylpyridin-2-amine is an organic compound characterized by a pyridine ring substituted with a chlorine atom and an amino group. The presence of the chlorine atom at the 4-position and a methyl group at the 6-position of the pyridine ring contributes to its unique chemical properties. This compound typically appears as a solid at room temperature and is soluble in polar organic solvents. It exhibits basic properties due to the amino group, which can participate in hydrogen bonding and act as a nucleophile in various chemical reactions. The compound is of interest in medicinal chemistry and may serve as a building block for the synthesis of pharmaceuticals or agrochemicals. Its reactivity can be influenced by the electron-withdrawing nature of the chlorine atom, which can affect the compound's behavior in electrophilic substitution reactions. Safety precautions should be taken when handling this substance, as it may pose health risks if ingested or inhaled.
Formula:C6H7ClN2
InChI:InChI=1/C6H7ClN2/c1-4-2-5(7)3-6(8)9-4/h2-3H,1H3,(H2,8,9)
SMILES:Cc1cc(cc(=N)[nH]1)Cl
Synonyms:- 2-Pyridinamine, 4-Chloro-6-Methyl-
- 4-Chloro-6-methylpyridin-2-amine
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Found 4 products.
2-Amino-4-chloro-6-picoline
CAS:Formula:C6H7ClN2Purity:97%Color and Shape:SolidMolecular weight:142.58624-Chloro-6-methylpyridin-2-amine
CAS:<p>4-Chloro-6-methylpyridin-2-amine</p>Formula:C6H7ClN2Purity:97%Color and Shape: grey solidMolecular weight:142.59g/mol2-Amino-4-chloro-6-methylpyridine
CAS:<p>2-Amino-4-chloro-6-methylpyridine (2ACP) is a molecule that has been studied by molecular modeling. This compound inhibits the enzyme tyrosine phosphatase, which is involved in the transmission of signals from outside the cell to inside the cell. 2ACP has a hydrogen bonding interaction with the catalytic site of the enzyme, which blocks its activity and prevents it from transmitting signals to other cells. 2ACP also has an inhibitory effect on fructus amomi and diamine tetraacetic acid (DTA), which are both enzymes involved in bacterial phosphorus metabolism. The structural analysis of 2ACP shows two protonated amino groups and one protonated pyridine group, which may explain its inhibitory effect on these enzymes.</p>Formula:C6H7ClN2Purity:Min. 95%Color and Shape:White PowderMolecular weight:142.59 g/mol2-Amino-4-chloro-6-picoline
CAS:Formula:C6H7ClN2Purity:97%Color and Shape:SolidMolecular weight:142.59



