CAS 20511-15-3
:4-Chloro-3-pyridinamine
Description:
4-Chloro-3-pyridinamine, with the CAS number 20511-15-3, is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. This compound features a chlorine atom and an amino group (-NH2) attached to the pyridine ring, specifically at the 4 and 3 positions, respectively. The presence of the chlorine atom contributes to its reactivity and potential applications in various chemical reactions, including nucleophilic substitutions. 4-Chloro-3-pyridinamine is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the amino group. It is often used in the synthesis of pharmaceuticals and agrochemicals, as well as in research settings for its potential biological activities. Safety precautions should be taken when handling this compound, as it may pose health risks, including irritation to the skin and eyes. Proper storage and disposal methods are essential to mitigate environmental impact and ensure safety.
Formula:C5H5ClN2
InChI:InChI=1S/C5H5ClN2/c6-4-1-2-8-3-5(4)7/h1-3H,7H2
InChI key:InChIKey=GTLFLMZOABSJSV-UHFFFAOYSA-N
SMILES:ClC=1C(N)=CN=CC1
Synonyms:- (4-Chloropyridin-3-yl)amine
- 3-Pyridinamine, 4-chloro-
- 4-Chloro-3-aminopyridine
- 4-Chloro-3-pyridinamine
- 4-Chloro-Pyridin-3-Ylamine
- 4-Chloropyrid-3-ylamine
- 4-Chloropyridin-3-Amine
- Pyridine, 3-amino-4-chloro-
- 3-Amino-4-chloropyridine
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Found 7 products.
3-Pyridinamine, 4-chloro-
CAS:Formula:C5H5ClN2Purity:98%Color and Shape:SolidMolecular weight:128.55963-Amino-4-chloropyridine
CAS:Formula:C5H5ClN2Purity:>98.0%(GC)(T)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:128.563-Amino-4-chloropyridine
CAS:<p>3-Amino-4-chloropyridine</p>Formula:C5H5ClN2Purity:98%Color and Shape:PowderMolecular weight:128.56g/mol3-Amino-4-chloropyridine
CAS:<p>3-Amino-4-chloropyridine is an organic compound with the molecular formula CHClN. It is a colorless solid that is soluble in organic solvents, such as diethyl ether and chloroform. 3-Amino-4-chloropyridine has been shown to be effective in cancer therapy by inhibiting ion channels, which are proteins that allow ions to pass through the cell membrane. This inhibition results in cell death due to lack of nutrients and oxygen. 3-Amino-4-chloropyridine inhibits the p2 receptor and induces apoptosis in cancer cells, which may be due to its ability to inhibit calcium influx and activate protein kinase C. 3-Amino-4-chloropyridine also has antiinflammatory effects by inhibiting prostaglandin synthesis.</p>Formula:C5H5ClN2Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:128.56 g/mol






