Ethyl indole-4-carboxylate in stock Factory
Ethyl indole-4-carboxylate
CAS: 50614-84-1
Molecular Formula: C11H11NO2
Ethyl indole-4-carboxylate in stock Factory - Names and Identifiers
| Name | Ethyl indole-4-carboxylate |
| Synonyms | Ethyl indole-4-carboxylate Ethyl 1H-indole-4-carboxylate Ethyl indole-4-carboxylate in stock Factory |
| CAS | 50614-84-1 |
| InChI | InChI=1/C11H11NO2/c1-2-14-11(13)9-4-3-5-10-8(9)6-7-12-10/h3-7,12H,2H2,1H3 |
Ethyl indole-4-carboxylate in stock Factory - Physico-chemical Properties
| Molecular Formula | C11H11NO2 |
| Molar Mass | 189.21 |
| Density | 1.210±0.06 g/cm3(Predicted) |
| Melting Point | 70-71 °C |
| Boling Point | 342.4±15.0 °C(Predicted) |
| Flash Point | 160.9°C |
| Vapor Presure | 7.57E-05mmHg at 25°C |
| pKa | 15.83±0.30(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
| Refractive Index | 1.62 |
Ethyl indole-4-carboxylate in stock Factory - Introduction
Ethyl indole-4-carboxylate, chemical formula C11H11NO2, is an organic compound. Its properties are as follows:
1. appearance: Ethyl indole-4-carboxylate is a colorless or light yellow liquid.
2. solubility: it can be dissolved in organic solvents, such as ethanol, ether and dichloromethane, insoluble in water.
3. melting point and boiling point: Ethyl indole-4-carboxylate has a melting point of about 57-60 degrees Celsius and a boiling point of about 285-286 degrees Celsius.
The main uses of Ethyl indole-4-carboxylate include:
1. Synthesis of indole compounds: Ethyl indole-4-carboxylate is an important intermediate for the synthesis of indole compounds. It can be used for the construction of indole ring by reaction with other compounds, and is used for the preparation of drugs, dyes and organic materials with indole structure.
2. Chemical research: Ethyl indole-4-carboxylate, as an organic synthesis reagent, can be used for the introduction of indole in organic synthesis reactions, such as in the field of natural product synthesis and drug research.
Ethyl indole-4-carboxylate preparation method mainly through the following steps:
1. First, indole is reacted with chloroformate to generate indole chloroformate.
2. Then, indole chloroformate was reacted with ethanol to obtain Ethyl indole-4-carboxylate.
When handling Ethyl indole-4-carboxylate, please note the following safety information:
1. Ethyl indole-4-carboxylate is irritating to skin, eyes and mucous membranes. Protective gloves, goggles and protective clothing should be worn during operation.
2. Avoid inhalation or contact with Ethyl indole-4-carboxylate during operation, and maintain a well-ventilated laboratory environment.
3. It should be stored in a cool, dry place, away from fire and oxidant.
4. Please dispose of the remaining Ethyl indole-4-carboxylate according to the correct waste disposal regulations.
This information is for reference only, and the specific use and treatment methods should be determined according to the actual situation and specific needs. It is recommended to follow relevant laboratory safety practices when using Ethyl indole-4-carboxylate.
1. appearance: Ethyl indole-4-carboxylate is a colorless or light yellow liquid.
2. solubility: it can be dissolved in organic solvents, such as ethanol, ether and dichloromethane, insoluble in water.
3. melting point and boiling point: Ethyl indole-4-carboxylate has a melting point of about 57-60 degrees Celsius and a boiling point of about 285-286 degrees Celsius.
The main uses of Ethyl indole-4-carboxylate include:
1. Synthesis of indole compounds: Ethyl indole-4-carboxylate is an important intermediate for the synthesis of indole compounds. It can be used for the construction of indole ring by reaction with other compounds, and is used for the preparation of drugs, dyes and organic materials with indole structure.
2. Chemical research: Ethyl indole-4-carboxylate, as an organic synthesis reagent, can be used for the introduction of indole in organic synthesis reactions, such as in the field of natural product synthesis and drug research.
Ethyl indole-4-carboxylate preparation method mainly through the following steps:
1. First, indole is reacted with chloroformate to generate indole chloroformate.
2. Then, indole chloroformate was reacted with ethanol to obtain Ethyl indole-4-carboxylate.
When handling Ethyl indole-4-carboxylate, please note the following safety information:
1. Ethyl indole-4-carboxylate is irritating to skin, eyes and mucous membranes. Protective gloves, goggles and protective clothing should be worn during operation.
2. Avoid inhalation or contact with Ethyl indole-4-carboxylate during operation, and maintain a well-ventilated laboratory environment.
3. It should be stored in a cool, dry place, away from fire and oxidant.
4. Please dispose of the remaining Ethyl indole-4-carboxylate according to the correct waste disposal regulations.
This information is for reference only, and the specific use and treatment methods should be determined according to the actual situation and specific needs. It is recommended to follow relevant laboratory safety practices when using Ethyl indole-4-carboxylate.
Last Update：2024-04-09 21:01:54
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Product Name: Ethyl 1H-indole-4-carboxylate Request for quotationCAS: 50614-84-1
Tel: 400-968-2212
Email: 3623107365@qq.com
Mobile: 18916960931
QQ: 3623107365
Wechat: 18916960931
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Product Name: Ethyl 1H-indole-4-carboxylate Visit Supplier Webpage Request for quotationCAS: 50614-84-1
Tel: +86-18821248368
Email: Int06@meryer.com
Mobile: +86-18821248368
QQ: 495145328
WhatsApp: +86-18821248368
Spot supply
Product Name: Ethyl 1H-indole-4-carboxylate Visit Supplier Webpage Request for quotationCAS: 50614-84-1
Tel: +86-400-900-4166
Email: product@acmec-e.com
Mobile: +86-18621343501
QQ: 2881950922
Wechat: 18621343501
WhatsApp: +86-18621343501
Product Name: Ethyl 1H-indole-4-carboxylate Visit Supplier Webpage Request for quotation
CAS: 50614-84-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
CAS: 50614-84-1
Tel: 18301782025
Email: 3008007409@qq.com
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