CAS 147249-42-1
:2-Aminomethyl-3,4-Dichloro-Phenylamine
Description:
2-Aminomethyl-3,4-Dichloro-Phenylamine, with the CAS number 147249-42-1, is an organic compound characterized by the presence of an amino group and dichlorinated phenyl moiety. This compound typically exhibits properties associated with amines, such as basicity and the ability to form hydrogen bonds. The dichloro substitution on the phenyl ring influences its reactivity and solubility, often making it less polar compared to non-chlorinated analogs. It may also exhibit biological activity, which can be of interest in pharmaceutical applications or as an intermediate in organic synthesis. The presence of the amino group suggests potential for nucleophilic reactions, while the dichloro groups can affect electronic properties and steric hindrance. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, 2-Aminomethyl-3,4-Dichloro-Phenylamine is a compound of interest in both industrial and research contexts, particularly in the development of new materials or pharmaceuticals.
Formula:C7H8Cl2N2
InChI:InChI=1/C7H8Cl2N2/c8-5-1-2-6(11)4(3-10)7(5)9/h1-2H,3,10-11H2
SMILES:c1cc(c(CN)c(c1Cl)Cl)N
Synonyms:- 2-(Aminomethyl)-3,4-dichloroaniline
- Benzenemethanamine, 6-Amino-2,3-Dichloro-
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Found 3 products.
(6-Amino-2,3-dichlorobenzyl)amine
CAS:Formula:C7H8Cl2N2Color and Shape:SolidMolecular weight:191.0578(6-Amino-2,3-dichlorobenzyl)amine
CAS:Controlled Product<p>Applications (6-Amino-2,3-dichlorobenzyl)amine is a reagent used in the synthesis of 3-Hydroxyanagrelide a derivative of Anagrelide (A637300), a drug used in the treatment of thrombocythemia.<br>References Scott, R. et al.: Heterocycles, 86, 1637 (2012);<br></p>Formula:C7H8Cl2N2Color and Shape:NeatMolecular weight:191.06


