6515-39-5

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
3,5-Dibromo-6-chloro-2-hydroxypyridine is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows it to be a key component in the development of various drugs and agricultural products.
Used in Antimicrobial and Anti-Fungal Applications:
3,5-Dibromo-6-chloro-2-hydroxypyridine has been studied for its potential as an antimicrobial and antifungal agent. Its ability to inhibit the growth of certain microorganisms makes it a valuable compound in the search for new treatments and preventative measures against infections.
Used in Material Science Applications:
3,5-Dibromo-6-chloro-2-hydroxypyridine has also been investigated for its potential use in material science applications. Its unique structure and properties may contribute to the development of new materials with specific characteristics for various industries and research areas.

Upstream product

• 16879-02-0 6-chloro-2-hydroxypyridine 

Relevant academic research and scientific papers

New Oxypyridinate Paddlewheel Ligands for Alkane-Soluble, Sterically-Protected Ru2(II,III) and Ru2(II,II) Complexes

The paddlewheel complex Ru2(chp)4Cl (1-Cl, chp = 6-chloro-2-oxypyridinate), upon reduction with Zn, has been previously shown to dimerize to [Ru2(chp)4]2 (2), blocking further chemistry at the Ru2(II,II) axial site [ Inorg. Chem. 2015, 54, 8571-8589 ]. Functionalization of the chp ligand at the 3 and 5 positions with either bromine (dbchpH = 3,5-dibromo-6-chloro-2-pyridone) or trimethylsilyl (TMS) groups (dsichpH = 6-chloro-3,5-bis(trimethylsilyl)-2-pyridone) allows for the preparation of the Ru2(II,II) paddlewheel complexes Ru2(dbchp)4 (3) and Ru2(dsichp)4 (6), respectively, neither of which shows evidence of dimerization. Though the utilization of 3 is limited due to insolubility, complex 6 is soluble even in typically non-coordinating solvents, forming a stable κ1-axial adduct in CH2Cl2 (6-CH2Cl2) and showing evidence of an axial interaction with n-decane. The first example of an axially free Ru2(II,II) complex with a 3A ground state is observed upon crystallization of 6 from benzene (6-C6D6). Complex 6 is accessed via Zn reduction of Ru2(dsichp)4Cl (4-Cl), which along with Ru2(dsichp)4N3 (4-N3), show similar structural and electronic properties to their non-TMS-substituted analogues, 1-Cl and 1-N3. Photolysis of 4-N3 in frozen solution generates Ru2(dsichp)4N (5); no N atom transfer to PPh3 is observed upon room temperature photolysis in fluid solution.