1H-Indol-3-ol, 6,7-dichloro-
1H-Indol-3-ol, 6,7-dichloro-
CAS: 384829-02-1
Molecular Formula: C8H5Cl2NO
1H-Indol-3-ol, 6,7-dichloro- - Names and Identifiers
| Name | 1H-Indol-3-ol, 6,7-dichloro- |
| Synonyms | 1H-Indol-3-ol, 6,7-dichloro- 1-Boc-6,7-Dichloro-1H-indol-3-ol tert-Butyl 6,7-dichloro-3-hydroxy-1H-indole-1-carboxylate |
| CAS | 384829-02-1 |
1H-Indol-3-ol, 6,7-dichloro- - Physico-chemical Properties
| Molecular Formula | C8H5Cl2NO |
| Molar Mass | 202.04 |
1H-Indol-3-ol, 6,7-dichloro- - Introduction
1H-Indol-3-ol, 6,7-dichloro-(1H-Indol-3-ol, 6,7-dichloro-, Boc protected) is an organic compound. It has the following properties:
1. Appearance: A white or light yellow solid.
2. molecular formula: C13H14Cl2N2O2.
3. Molecular weight: 303.17g/mol.
4. solubility: soluble in some organic solvents, such as dimethylformamide and ethyl formate.
1H-Indol-3-ol, 6,7-dichloro-is mainly used in the field of organic synthesis, as an intermediate or starting material to participate in a variety of reactions, such as hydroxyacyl chloride substitution, nucleophilic substitution, etc. It can be used in the synthesis of indole-containing structures of natural products and drug molecules.
The method of preparing 1H-Indol-3-ol, 6,7-dichloro-can use the indole-3-hydroxy compound to react with dichlorocarbonate, and then perform the protection reaction by adding a protecting reagent (such as t-butyl dimethyl carbaron anhydride).
Regarding safety information, the toxicity data of 1H-Indol-3-ol, 6,7-dichloro-is limited, so appropriate laboratory safety measures need to be taken. Personal protective equipment such as lab gloves, glasses and lab coats should be worn during operation. Avoid inhalation, skin contact and ingestion. Regularly ventilate and observe relevant safety procedures. If exposed or inhaled, seek medical attention immediately.
1. Appearance: A white or light yellow solid.
2. molecular formula: C13H14Cl2N2O2.
3. Molecular weight: 303.17g/mol.
4. solubility: soluble in some organic solvents, such as dimethylformamide and ethyl formate.
1H-Indol-3-ol, 6,7-dichloro-is mainly used in the field of organic synthesis, as an intermediate or starting material to participate in a variety of reactions, such as hydroxyacyl chloride substitution, nucleophilic substitution, etc. It can be used in the synthesis of indole-containing structures of natural products and drug molecules.
The method of preparing 1H-Indol-3-ol, 6,7-dichloro-can use the indole-3-hydroxy compound to react with dichlorocarbonate, and then perform the protection reaction by adding a protecting reagent (such as t-butyl dimethyl carbaron anhydride).
Regarding safety information, the toxicity data of 1H-Indol-3-ol, 6,7-dichloro-is limited, so appropriate laboratory safety measures need to be taken. Personal protective equipment such as lab gloves, glasses and lab coats should be worn during operation. Avoid inhalation, skin contact and ingestion. Regularly ventilate and observe relevant safety procedures. If exposed or inhaled, seek medical attention immediately.
Last Update：2024-04-09 20:49:11
