1H-Indole-2-carboxylic acid, 3-hydroxy-5-methoxy-, ethyl ester
ethyl 3-hydroxy-5-methoxy-1H-indole-2-carboxylate
CAS: 318292-61-4
Molecular Formula: C12H13NO4
1H-Indole-2-carboxylic acid, 3-hydroxy-5-methoxy-, ethyl ester - Names and Identifiers
| Name | ethyl 3-hydroxy-5-methoxy-1H-indole-2-carboxylate |
| Synonyms | LogP ethyl 3-hydroxy-5-methoxy-1H-indole-2-carboxylate Ethyl 3-hydroxy-5-methoxy-1H-indole-2-carboxylate 1H-Indole-2-carboxylic acid, 3-hydroxy-5-methoxy-, ethyl ester |
| CAS | 318292-61-4 |
| InChI | InChI=1/C12H13NO4/c1-3-17-12(15)10-11(14)8-6-7(16-2)4-5-9(8)13-10/h4-6,13-14H,3H2,1-2H3 |
1H-Indole-2-carboxylic acid, 3-hydroxy-5-methoxy-, ethyl ester - Physico-chemical Properties
| Molecular Formula | C12H13NO4 |
| Molar Mass | 235.24 |
| Density | 1.316 |
| Boling Point | 405.583°C at 760 mmHg |
| Flash Point | 199.09°C |
| Vapor Presure | 0mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.629 |
1H-Indole-2-carboxylic acid, 3-hydroxy-5-methoxy-, ethyl ester - Introduction
ethyl, chemical formula C13H13NO4, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: It is a white or off-white crystalline solid.
-Solubility: Soluble in ethanol, methanol and chloroform, slightly soluble in water.
Use:
-Drug synthesis: ethyl is an important intermediate and is widely used in drug synthesis. It can be used to prepare biologically active indole derivatives, such as anticancer drugs, anti-tuberculosis drugs, etc.
-Scientific research: As an important compound in organic synthetic chemistry, it is also used in various scientific research fields.
Method:
ethyl L is generally synthesized by the following reaction steps:
1. First, Nitro indole is obtained by nitration reaction.
2. Then, nitroindole reacts with nitroso ethanol to generate ethyl nitroso acetate.
3. Finally, the acid conversion reaction of nitrosyl ethyl acetate and nitrosyl ethanol is obtained.
Safety Information:
-Pay attention to personal protective measures during operation, such as wearing chemical protective glasses, respiratory protective equipment and chemical protective clothing.
-Avoid inhalation of dust, contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
-During storage and handling, avoid contact with oxidants, strong acids and strong bases to avoid dangerous reactions.
-If you need to dispose of waste, please comply with local regulations and dispose of it properly.
Nature:
-Appearance: It is a white or off-white crystalline solid.
-Solubility: Soluble in ethanol, methanol and chloroform, slightly soluble in water.
Use:
-Drug synthesis: ethyl is an important intermediate and is widely used in drug synthesis. It can be used to prepare biologically active indole derivatives, such as anticancer drugs, anti-tuberculosis drugs, etc.
-Scientific research: As an important compound in organic synthetic chemistry, it is also used in various scientific research fields.
Method:
ethyl L is generally synthesized by the following reaction steps:
1. First, Nitro indole is obtained by nitration reaction.
2. Then, nitroindole reacts with nitroso ethanol to generate ethyl nitroso acetate.
3. Finally, the acid conversion reaction of nitrosyl ethyl acetate and nitrosyl ethanol is obtained.
Safety Information:
-Pay attention to personal protective measures during operation, such as wearing chemical protective glasses, respiratory protective equipment and chemical protective clothing.
-Avoid inhalation of dust, contact with skin and eyes. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
-During storage and handling, avoid contact with oxidants, strong acids and strong bases to avoid dangerous reactions.
-If you need to dispose of waste, please comply with local regulations and dispose of it properly.
Last Update：2024-04-09 21:01:54
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Product Name: Ethyl 3-hydroxy-5-methoxy-1H-indole-2-carboxylate Visit Supplier Webpage Request for quotation
CAS: 318292-61-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 318292-61-4
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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