4-Bromo-6-iodo-1H-indazole
4-Bromo-6-iodo-1H-indazole
CAS: 885518-97-8
Molecular Formula: C7H4BrIN2
4-Bromo-6-iodo-1H-indazole - Names and Identifiers
| Name | 4-Bromo-6-iodo-1H-indazole |
| Synonyms | 4-bromo-6-iodoindazole 4-Bromo-6-iodo-1H-indazole 1H-Indazole,4-broMo-6-iodo- 1H-Indazole, 4-broMo-6-iodo- |
| CAS | 885518-97-8 |
| EINECS | 200-258-5 |
| InChI | InChI=1S/C7H4BrIN2/c8-6-1-4(9)2-7-5(6)3-10-11-7/h1-3H,(H,10,11) |
4-Bromo-6-iodo-1H-indazole - Physico-chemical Properties
| Molecular Formula | C7H4BrIN2 |
| Molar Mass | 322.93 |
| Density | 2.421±0.06 g/cm3(Predicted) |
| Boling Point | 410.4±30.0 °C(Predicted) |
| pKa | 11.74±0.40(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
4-Bromo-6-iodo-1H-indazole - Introduction
4-Bromo-6-iodo-1H-indazole is an indazole derivative containing bromine and iodine. It has the following properties:
Appearance: colorless crystal or white solid
Molecular formula: C7H3BrIN
Molecular weight: 340.91g/mol
4-Bromo-6-iodo-1H-indazole can be used for various reactions in organic synthesis, such as aromatic interconversion reaction, oxidation reaction and reduction reaction. Because of its special structure and chemical properties, it also has certain applications in drug research and pesticide research and development.
The method for producing the same can be synthesized by reacting indazole with sulfoxide bromide and sulfoxide iodide. This reaction is carried out under suitable solvent and temperature conditions.
Regarding safety information, the toxicological data on 4-Bromo-6-iodo-1H-indazole is limited, so it needs to be handled with care. During use and handling, laboratory safety procedures should be followed and appropriate personal protective measures should be taken, such as wearing gloves, goggles and laboratory coats. In addition, it should be stored in a dry, cool place and separated from incompatible substances.
Appearance: colorless crystal or white solid
Molecular formula: C7H3BrIN
Molecular weight: 340.91g/mol
4-Bromo-6-iodo-1H-indazole can be used for various reactions in organic synthesis, such as aromatic interconversion reaction, oxidation reaction and reduction reaction. Because of its special structure and chemical properties, it also has certain applications in drug research and pesticide research and development.
The method for producing the same can be synthesized by reacting indazole with sulfoxide bromide and sulfoxide iodide. This reaction is carried out under suitable solvent and temperature conditions.
Regarding safety information, the toxicological data on 4-Bromo-6-iodo-1H-indazole is limited, so it needs to be handled with care. During use and handling, laboratory safety procedures should be followed and appropriate personal protective measures should be taken, such as wearing gloves, goggles and laboratory coats. In addition, it should be stored in a dry, cool place and separated from incompatible substances.
Last Update：2024-04-09 20:52:54
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