4,5-Dibromo-1H-indazole is a chemical compound characterized by its indazole core, which consists of a five-membered ring fused to a six-membered aromatic ring. The presence of two bromine atoms at the 4 and 5 positions of the indazole structure significantly influences its chemical properties, including its reactivity and solubility. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. The bromine substituents can enhance the compound's lipophilicity, potentially affecting its bioavailability and pharmacokinetics. Additionally, 4,5-Dibromo-1H-indazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

4,5-Dibromo-1H-indazole

1351668-28-4: 4,5-Dibromo-1H-indazole is a chemical compound characterized by its indazole core, which consists of a five-membered ring fused to a six-membered aromatic ring. The presence of two bromine atoms at the 4 and 5 positions of the indazole structure significantly influences its chemical properties, including its reactivity and solubility. This compound is typically a solid at room temperature and may exhibit a range of colors depending on its purity and crystalline form. It is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. The bromine substituents can enhance the compound's lipophilicity, potentially affecting its bioavailability and pharmacokinetics. Additionally, 4,5-Dibromo-1H-indazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, making it a versatile intermediate in organic synthesis. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks.

CAS 1351668-28-4

4,5-Dibromo-1H-indazole

4,5-Dibromo-1H-indazole

Ref: IN-DA01LNNO

4,5-Dibromo-1H-indazole

Ref: 54-OR1038797

4,5-DIBROMO-1H-INDAZOLE

Ref: 10-F854721