1H-Indole, 5-bromo-3-iodo-
5-bromo-3-iodo-1H-indole
CAS: 868694-19-3
Molecular Formula: C8H5BrIN
1H-Indole, 5-bromo-3-iodo- - Names and Identifiers
| Name | 5-bromo-3-iodo-1H-indole |
| Synonyms | 5-bromo-3-iodo-1H-indole 1H-Indole, 5-broMo-3-iodo- 1H-Indole, 5-bromo-3-iodo- |
| CAS | 868694-19-3 |
| InChI | InChI=1S/C8H5BrIN/c9-5-1-2-8-6(3-5)7(10)4-11-8/h1-4,11H |
1H-Indole, 5-bromo-3-iodo- - Physico-chemical Properties
| Molecular Formula | C8H5BrIN |
| Molar Mass | 321.94 |
| Storage Condition | Room Temprature |
1H-Indole, 5-bromo-3-iodo- - Introduction
5-bromo-3-iodo-1H-indole(5-bromo-3-iodo-1H-indole) is an organic compound with the chemical formula C8H5BrIN. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: The pure product is a white crystalline solid, but the common commercial sample is a light yellow or yellow solid.
-Solubility: 5-bromo-3-iodo-1H-indole has good solubility in common organic solvents, such as ammonia and potassium hydroxide solution.
Use:
-Chemical synthesis: 5-bromo-3-iodo-1H-indole can be used as a starting material for the synthesis of other organic compounds, such as derived indole compounds and other heterocyclic compounds.
-Drug research: 5-bromo-3-iodo-1H-indole can be used in drug research as an intermediate in organic synthesis.
Preparation Method:
5-bromo-3-iodo-1H-indole can be prepared by the following steps:
1. Indole is reacted with carbon dibromide to give 5-bromo-1H-indole (5-bromo-1H-indole).
2. 5-bromo-1H-indole is reacted with sulfuric acid and sodium iodide to obtain 5-bromo-3-iodo-1H-indole.
Safety Information:
- 5-bromo-3-iodo-1H-indole is an organic compound that needs to be handled carefully.
-It may cause irritation to the eyes, skin and respiratory tract, so use safety measures such as gloves and goggles.
-During operation and storage, it is necessary to avoid contact with oxidants, acids and high temperatures.
-When using this compound, follow appropriate laboratory safety procedures.
Nature:
-Appearance: The pure product is a white crystalline solid, but the common commercial sample is a light yellow or yellow solid.
-Solubility: 5-bromo-3-iodo-1H-indole has good solubility in common organic solvents, such as ammonia and potassium hydroxide solution.
Use:
-Chemical synthesis: 5-bromo-3-iodo-1H-indole can be used as a starting material for the synthesis of other organic compounds, such as derived indole compounds and other heterocyclic compounds.
-Drug research: 5-bromo-3-iodo-1H-indole can be used in drug research as an intermediate in organic synthesis.
Preparation Method:
5-bromo-3-iodo-1H-indole can be prepared by the following steps:
1. Indole is reacted with carbon dibromide to give 5-bromo-1H-indole (5-bromo-1H-indole).
2. 5-bromo-1H-indole is reacted with sulfuric acid and sodium iodide to obtain 5-bromo-3-iodo-1H-indole.
Safety Information:
- 5-bromo-3-iodo-1H-indole is an organic compound that needs to be handled carefully.
-It may cause irritation to the eyes, skin and respiratory tract, so use safety measures such as gloves and goggles.
-During operation and storage, it is necessary to avoid contact with oxidants, acids and high temperatures.
-When using this compound, follow appropriate laboratory safety procedures.
Last Update：2024-04-09 20:49:11
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CAS: 868694-19-3
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CAS: 868694-19-3
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