1-(2-Bromo-acetyl)-piperidine-4-carboxylic acid ethyl ester
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate
CAS: 102302-12-5
Molecular Formula: C10H16BrNO3
1-(2-Bromo-acetyl)-piperidine-4-carboxylic acid ethyl ester - Names and Identifiers
1-(2-Bromo-acetyl)-piperidine-4-carboxylic acid ethyl ester - Physico-chemical Properties
| Molecular Formula | C10H16BrNO3 |
| Molar Mass | 278.14 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD12026649 |
1-(2-Bromo-acetyl)-piperidine-4-carboxylic acid ethyl ester - Introduction
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate in ethyl acetate is an organic compound with the chemical formula C12H17BrNO3.
Nature:
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate in ethyl acetate is a white solid with bromine absorption and pungent odor. It has a melting point of about 75-77°C, a low solubility, and is soluble in organic solvents such as methanol and dichloromethane.
Use:
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate from ethyl acetate is commonly used as an intermediate in organic synthesis and has important applications in the field of medicine. It can be used to synthesize various drugs and bioactive molecules, such as antibacterial agents, anti-inflammatory agents and analgesics.
Preparation Method:
From the perspective of chemical synthesis, ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate of ethyl acetate can be obtained by reacting bromoacetic acid with ethyl 4-piperidinecarboxylate. This reaction needs to be carried out at an appropriate temperature and under appropriate conditions, and usually requires the use of an organic solvent and a catalyst to facilitate the reaction.
Safety Information:
ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate in ethyl acetate should follow the relevant safety procedures during operation. It is an organic compound that is potentially dangerous. Contact with skin, eyes or respiratory tract may cause irritation or injury. Eating or inhaling dust should be avoided. Wear appropriate protective equipment such as gloves, goggles and breathing masks during use. In the event of an accident, immediately flush the affected area with plenty of clean water and seek medical attention. The operation should be carried out in a well-ventilated area to ensure safety.
Nature:
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate in ethyl acetate is a white solid with bromine absorption and pungent odor. It has a melting point of about 75-77°C, a low solubility, and is soluble in organic solvents such as methanol and dichloromethane.
Use:
Ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate from ethyl acetate is commonly used as an intermediate in organic synthesis and has important applications in the field of medicine. It can be used to synthesize various drugs and bioactive molecules, such as antibacterial agents, anti-inflammatory agents and analgesics.
Preparation Method:
From the perspective of chemical synthesis, ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate of ethyl acetate can be obtained by reacting bromoacetic acid with ethyl 4-piperidinecarboxylate. This reaction needs to be carried out at an appropriate temperature and under appropriate conditions, and usually requires the use of an organic solvent and a catalyst to facilitate the reaction.
Safety Information:
ethyl 1-(2-bromoacetyl)-4-piperidinecarboxylate in ethyl acetate should follow the relevant safety procedures during operation. It is an organic compound that is potentially dangerous. Contact with skin, eyes or respiratory tract may cause irritation or injury. Eating or inhaling dust should be avoided. Wear appropriate protective equipment such as gloves, goggles and breathing masks during use. In the event of an accident, immediately flush the affected area with plenty of clean water and seek medical attention. The operation should be carried out in a well-ventilated area to ensure safety.
Last Update：2024-04-09 02:00:57
