| Chemical Name: | 5-chloroquinolin-4-amine |
| CAS Number: | 92385-37-0 |
| Product Number: | AG00GRVP(AGN-PC-09RRL8) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C9H7ClN2 |
| Molecular Weight: | 178.6183 |
5-Chloro-4-quinolinamine is a versatile compound widely used in chemical synthesis for its unique properties. Its application in organic chemistry mainly revolves around its ability to serve as a key building block for the synthesis of various pharmaceutical and agrochemical compounds. The presence of the chloro and amino groups in its structure makes it a valuable intermediate in the preparation of a wide range of biologically active molecules.In chemical synthesis, 5-Chloro-4-quinolinamine can undergo various types of reactions such as nucleophilic substitution, condensation, and cyclization to form complex molecular structures. It can be utilized as a precursor for the synthesis of quinoline derivatives, which are important pharmacophores found in many drugs targeting various diseases. Additionally, its reactivity allows for the introduction of diverse functional groups, enabling the customization of the final products for specific applications.Moreover, 5-Chloro-4-quinolinamine plays a crucial role in the development of novel compounds with biological activities. By incorporating this compound into synthetic pathways, chemists can access a broad chemical space and explore new chemical entities with potential therapeutic properties. Overall, the utility of 5-Chloro-4-quinolinamine in chemical synthesis extends to the creation of valuable intermediates and final products with significant relevance in medicinal chemistry and agriculture.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
