Ethyloxindole-6-carboxylate
Ethyloxindole-6-carboxylate
CAS: 107516-75-6
Molecular Formula: C14H15NO4
Ethyloxindole-6-carboxylate - Names and Identifiers
Ethyloxindole-6-carboxylate - Physico-chemical Properties
| Molecular Formula | C14H15NO4 |
| Molar Mass | 261.27 |
| Density | 1.240±0.06 g/cm3(Predicted) |
| Melting Point | 119-121℃ |
| Boling Point | 420.2±25.0 °C(Predicted) |
| Appearance | Yellow solid |
| pKa | 13.84±0.30(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
| MDL | MFCD03411566 |
Ethyloxindole-6-carboxylate - Introduction
Ethyloxindole-6-carboxylate is an organic compound with the chemical formula C12H11NO3. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
Ethyloxindole-6-carboxylate is a white crystalline solid that is stable at room temperature. It has low solubility, is insoluble in water, and is soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
Ethyloxindole-6-carboxylate have a variety of applications in the field of organic synthesis. It is a derivative of indolinone and can be used as a synthetic intermediate for the preparation of biologically active compounds. It has potential applications in the field of drug development, and may be used to synthesize antibacterial, antiviral and antitumor drugs.
Method:
The preparation of Ethyloxindole-6-carboxylate can be obtained by reacting indolinone with ethyl pyruvate under alkaline conditions. First, indolinone and ethyl pyruvate are added to an alkaline solution, reacted under appropriate reaction conditions, and the reaction product is crystallized and purified to obtain the target compound.
Safety Information:
Ethyloxindole-6-carboxylate safety data is limited. Relevant laboratory safety guidelines and procedures should be followed when handling and using compounds. Due to the lack of relevant toxicological and safety data, it is recommended to take appropriate personal protective measures when using it to avoid direct contact with the skin or inhalation of its dust or vapor. If any unexpected exposure or discomfort occurs, medical advice should be sought immediately.
Nature:
Ethyloxindole-6-carboxylate is a white crystalline solid that is stable at room temperature. It has low solubility, is insoluble in water, and is soluble in organic solvents such as ethanol and dimethyl sulfoxide.
Use:
Ethyloxindole-6-carboxylate have a variety of applications in the field of organic synthesis. It is a derivative of indolinone and can be used as a synthetic intermediate for the preparation of biologically active compounds. It has potential applications in the field of drug development, and may be used to synthesize antibacterial, antiviral and antitumor drugs.
Method:
The preparation of Ethyloxindole-6-carboxylate can be obtained by reacting indolinone with ethyl pyruvate under alkaline conditions. First, indolinone and ethyl pyruvate are added to an alkaline solution, reacted under appropriate reaction conditions, and the reaction product is crystallized and purified to obtain the target compound.
Safety Information:
Ethyloxindole-6-carboxylate safety data is limited. Relevant laboratory safety guidelines and procedures should be followed when handling and using compounds. Due to the lack of relevant toxicological and safety data, it is recommended to take appropriate personal protective measures when using it to avoid direct contact with the skin or inhalation of its dust or vapor. If any unexpected exposure or discomfort occurs, medical advice should be sought immediately.
Last Update：2024-04-09 21:01:54
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View History
Ethyloxindole-6-carboxylate
(S)-1-(噻吩-2-基)乙胺
氯化钾
3-(acetyloxy)-2-methylbenzoic acid
N-Tert-Butyloxycarbonyl-Isonipecotic Acid
Ropivacaine base Mepivacaine HCL
(S)-1-(噻吩-2-基)乙胺
氯化钾
3-(acetyloxy)-2-methylbenzoic acid
N-Tert-Butyloxycarbonyl-Isonipecotic Acid
Ropivacaine base Mepivacaine HCL