CAS 13096-96-3: 4-CHLORO (1H)INDAZOLE

Description: 4-Chloro(1H)indazole is a heterocyclic organic compound characterized by its indazole structure, which consists of a fused benzene and pyrazole ring. The presence of a chlorine atom at the 4-position of the indazole ring significantly influences its chemical properties and reactivity. This compound is typically a white to off-white solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. It may exhibit properties such as anti-inflammatory, anti-cancer, or antimicrobial effects, making it of interest in drug discovery. The compound is soluble in organic solvents, and its reactivity can be attributed to the presence of the chlorine substituent, which can participate in nucleophilic substitution reactions. Additionally, 4-chloro(1H)indazole can serve as a building block for synthesizing more complex molecules in organic synthesis. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity and environmental impact.

Formula: C₇H₅ClN₂

InChI: InChI=1/C7H5ClN2/c8-6-2-1-3-7-5(6)4-9-10-7/h1-4H,(H,9,10)

Synonyms:

• 4-Chloro-1H-indazole

1H-Indazole, 4-chloro-

CAS: 13096-96-3

• Formula: C₇H₅ClN₂
• Purity: 97%
• Color and Shape: Solid
• Molecular weight: 152.581

4-Chloro-1H-indazole

CAS: 13096-96-3

• Formula: C₇H₅ClN₂
• Purity: By hplc: 99.9% by area (Typical Value in Batch COA)
• Color and Shape: off white solid
• Molecular weight: 152.58g/mol

4-Chloro-1H-indazole

CAS: 13096-96-3

• Purity: 97.0%
• Color and Shape: Solid
• Molecular weight: 152.5800018310547

4-Chloro-1H-indazole

CAS: 13096-96-3

4-Chloro-1H-indazole is an organic compound that has potent anticancer activity. It has been shown to …

• Formula: C₇H₅ClN₂
• Purity: Min. 95%
• Molecular weight: 152.58 g/mol