Ethyl5-bromo-1H-indole-3-carboxylate
Ethyl5-bromo-1H-indole-3-carboxylate
CAS: 103858-54-4
Molecular Formula: C11H10BrNO2
Ethyl5-bromo-1H-indole-3-carboxylate - Names and Identifiers
Ethyl5-bromo-1H-indole-3-carboxylate - Physico-chemical Properties
| Molecular Formula | C11H10BrNO2 |
| Molar Mass | 268.11 |
Ethyl5-bromo-1H-indole-3-carboxylate - Introduction
Ethyl5-bromo-1H-indole-3-carboxylate is a compound with the chemical formula C12H10BrNO2. The following is a description of its nature, use, formulation and safety information:
Nature:
- Ethyl5-bromo-1H-indole-3-carboxylate is a colorless to pale yellow solid with similar odor characteristics.
-It is stable at room temperature, but may decompose under high temperature and oxidation conditions.
-its solubility is good, soluble in a variety of organic solvents, such as ethanol, ether and dichloromethane.
Use:
- Ethyl5-bromo-1H-indole-3-carboxylate is an important intermediate in organic synthesis and can be used to synthesize other biologically active compounds.
-It has a wide range of applications in pharmaceutical chemistry, materials science and other fields.
Method:
-The synthesis of Ethyl5-bromo-1H-indole-3-carboxylate is usually carried out by an ethyl esterification reaction.
-The specific preparation method can be achieved by reacting 5-bromoindole-3-carboxylic acid with ethanol in the presence of a certain catalyst.
Safety Information:
-The Ethyl5-bromo-1H-indole-3-carboxylate will not cause serious health hazards under normal operating conditions.
-However, it is still necessary to follow regular handling and storage safety measures for chemicals, avoiding contact with eyes, skin and respiratory tract.
-Wear appropriate personal protective equipment, such as lab gloves, goggles and protective clothing, when performing relevant experiments or operations.
Nature:
- Ethyl5-bromo-1H-indole-3-carboxylate is a colorless to pale yellow solid with similar odor characteristics.
-It is stable at room temperature, but may decompose under high temperature and oxidation conditions.
-its solubility is good, soluble in a variety of organic solvents, such as ethanol, ether and dichloromethane.
Use:
- Ethyl5-bromo-1H-indole-3-carboxylate is an important intermediate in organic synthesis and can be used to synthesize other biologically active compounds.
-It has a wide range of applications in pharmaceutical chemistry, materials science and other fields.
Method:
-The synthesis of Ethyl5-bromo-1H-indole-3-carboxylate is usually carried out by an ethyl esterification reaction.
-The specific preparation method can be achieved by reacting 5-bromoindole-3-carboxylic acid with ethanol in the presence of a certain catalyst.
Safety Information:
-The Ethyl5-bromo-1H-indole-3-carboxylate will not cause serious health hazards under normal operating conditions.
-However, it is still necessary to follow regular handling and storage safety measures for chemicals, avoiding contact with eyes, skin and respiratory tract.
-Wear appropriate personal protective equipment, such as lab gloves, goggles and protective clothing, when performing relevant experiments or operations.
Last Update：2024-04-09 02:00:51
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Product Name: ethyl 5-bromo-1H-indole-3-carboxylate Visit Supplier Webpage Request for quotationCAS: 103858-54-4
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Product Name: RARECHEM AL BI 0374 Visit Supplier Webpage Request for quotation
CAS: 103858-54-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 103858-54-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
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