CAS 7709-13-9
:4-chloro-1,3,5-triazin-2-amine
Description:
4-Chloro-1,3,5-triazin-2-amine, with the CAS number 7709-13-9, is a heterocyclic organic compound characterized by a triazine ring structure. This compound features a chlorine atom and an amino group attached to the triazine ring, which contributes to its reactivity and potential applications. It is typically a white to light yellow crystalline solid that is soluble in polar solvents. The presence of the amino group allows for hydrogen bonding, enhancing its solubility and reactivity in various chemical reactions. This compound is often utilized in agricultural chemistry, particularly as a herbicide or in the synthesis of other chemical products. Its chlorinated structure can impart specific biological activity, making it of interest in both industrial and research settings. Safety considerations should be taken into account, as with many chlorinated compounds, due to potential toxicity and environmental impact. Proper handling and disposal methods are essential to mitigate any risks associated with its use.
Formula:C3H3ClN4
InChI:InChI=1/C3H3ClN4/c4-2-6-1-7-3(5)8-2/h1H,(H2,5,6,7,8)
SMILES:c1nc(Cl)nc(=N)[nH]1
Synonyms:- 1,3,5-Triazin-2-amine, 4-chloro-
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Found 4 products.
4-AMino-2-chloro-1,3,5-triazine
CAS:Formula:C3H3ClN4Purity:95%Color and Shape:SolidMolecular weight:130.53574-Amino-2-chloro-1,3,5-triazine
CAS:<p>4-Amino-2-chloro-1,3,5-triazine is a potent soil microorganism that utilizes reactive amines and naphthalene as its sole carbon source. It is a polymorphic species that can form four different types of crystals, which are typically found in untreated soil samples. 4-Amino-2-chloro-1,3,5-triazine can be used for the biotransformation of chaperones and detoxification of xenobiotics. It is also capable of deaminating hydrophobic compounds.</p>Formula:C3H3ClN4Purity:Min. 95%Molecular weight:130.54 g/mol




