1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3...
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-
CAS: 876461-55-1
Molecular Formula: C13H18N2O2
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3... - Names and Identifiers
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3... - Physico-chemical Properties
| Molecular Formula | C13H18N2O2 |
| Molar Mass | 234.29 |
| Density | 1.151±0.06 g/cm3(Predicted) |
| Boling Point | 367.2±42.0 °C(Predicted) |
| pKa | 10.33±0.20(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3... - Risk and Safety
| Safety Description | 24/25 - Avoid contact with skin and eyes. |
| HS Code | 29333990 |
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3... - Introduction
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl-ester, (3S)-, also known as 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl-ester, (3S)-, is an organic compound. Its structure contains an amino group and a piperidine ring, and a benzoyl group (Cbz group) is attached to the amino group. The specific nature is as follows:
1. Appearance: 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl-ester, (3S)-is a colorless solid.
2. Solubility: It is easy to dissolve in common polar solvents, such as ethanol, dimethyl amide and dichloromethane.
3. Melting point: Its melting point is about 60-70 degrees Celsius.
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-are mainly used in the following aspects:
1. Biological activity research: It can be used as an organic synthesis intermediate for the synthesis of various biologically active compounds, such as drugs, pesticides, etc.
2. Catalyst: It can also be used as a catalyst to participate in organic synthesis reactions and promote the progress of specific chemical reactions.
The method of preparing 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-is generally realized by chemical synthesis, including the following steps:
1. piperidine is reacted with bromoacetic acid to obtain piperidine -1-ethyl carboxylate.
2. Reduction of piperidine -1-ethyl carboxylate to piperidine -1-ethanol and acylation to piperidine -1-acetic acid.
3. piperidine -1-acetic acid and benzoyl chloride are reacted to generate 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-.
Regarding safety information, due to the complex nature of chemical substances, exact safety information needs to be evaluated on a case-by-case basis. But in general, chemical substances should pay attention to the following safety operations:
1. avoid direct contact with skin and eyes, avoid inhaling its dust or gas.
2. During operation, appropriate laboratory protective equipment should be worn, such as gloves, goggles, and laboratory atmospheric ventilation devices.
3. storage and handling, should follow the correct chemical management methods and regulations.
Every laboratory and user of chemicals should use chemicals appropriately in a safe environment according to specific needs and conditions. Before using any chemical substance, it is recommended to consult the safety data sheet (MSDS) of the chemical and follow the relevant safety practices.
1. Appearance: 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl-ester, (3S)-is a colorless solid.
2. Solubility: It is easy to dissolve in common polar solvents, such as ethanol, dimethyl amide and dichloromethane.
3. Melting point: Its melting point is about 60-70 degrees Celsius.
1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-are mainly used in the following aspects:
1. Biological activity research: It can be used as an organic synthesis intermediate for the synthesis of various biologically active compounds, such as drugs, pesticides, etc.
2. Catalyst: It can also be used as a catalyst to participate in organic synthesis reactions and promote the progress of specific chemical reactions.
The method of preparing 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-is generally realized by chemical synthesis, including the following steps:
1. piperidine is reacted with bromoacetic acid to obtain piperidine -1-ethyl carboxylate.
2. Reduction of piperidine -1-ethyl carboxylate to piperidine -1-ethanol and acylation to piperidine -1-acetic acid.
3. piperidine -1-acetic acid and benzoyl chloride are reacted to generate 1-Piperidinecarboxylicacid, 3-amino-, phenylmethyl ester, (3S)-.
Regarding safety information, due to the complex nature of chemical substances, exact safety information needs to be evaluated on a case-by-case basis. But in general, chemical substances should pay attention to the following safety operations:
1. avoid direct contact with skin and eyes, avoid inhaling its dust or gas.
2. During operation, appropriate laboratory protective equipment should be worn, such as gloves, goggles, and laboratory atmospheric ventilation devices.
3. storage and handling, should follow the correct chemical management methods and regulations.
Every laboratory and user of chemicals should use chemicals appropriately in a safe environment according to specific needs and conditions. Before using any chemical substance, it is recommended to consult the safety data sheet (MSDS) of the chemical and follow the relevant safety practices.
Last Update：2024-04-10 22:41:30
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