6-Chloroisoquinoline is a heterocyclic organic compound characterized by a fused ring structure that includes a benzene ring and a pyridine ring, with a chlorine substituent at the 6-position of the isoquinoline framework. Its molecular formula is C9H6ClN, indicating the presence of nine carbon atoms, six hydrogen atoms, one nitrogen atom, and one chlorine atom. This compound typically appears as a pale yellow to light brown solid and is known for its aromatic properties, which contribute to its stability and reactivity. 6-Chloroisoquinoline is of interest in medicinal chemistry and organic synthesis, often serving as a building block for the development of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the presence of the chlorine atom, which can participate in various substitution reactions. Additionally, the nitrogen atom in the isoquinoline structure can engage in coordination with metal ions, making it relevant in coordination chemistry. Safety data should be consulted for handling and storage, as with any chemical substance.

6-chloroisoquinoline

62882-02-4: Isoquinoline, 6-Chloro-, 6-Chloroisoquinoline

6-Chloroisoquinoline

6-Chloroisoquinoline is an enantioenriched compound that is used as an activator in organic synthesis. It has been shown to be effective for the asymmetric alkynylation of a variety of alkenes, including allenes and cyclohexenes. The high yields observed with this compound are attributed to its ability to act as an additive. 6-Chloroisoquinoline also exhibits the ability to activate a wide range of functional groups, such as ketones, nitriles, sulfonates, and esters.

CAS 62882-02-4: 6-chloroisoquinoline

6-Chloroisoquinoline

Ref: 54-OR300089

6-Chloroisoquinoline

Ref: 10-F049138

6-Chloroisoquinoline

Ref: 3D-FC42310

6-Chloroisoquinoline

Ref: IN-DA003N6K