benzyl (3S)-piperidin-3-ylcarbamate
benzyl (3S)-piperidin-3-ylcarbamate
CAS: 478646-33-2
Molecular Formula: C13H18N2O2
benzyl (3S)-piperidin-3-ylcarbamate - Names and Identifiers
| Name | benzyl (3S)-piperidin-3-ylcarbamate |
| Synonyms | (S)-3-(Cbz-aMino)piperidine (S)-3-(Cbz-aMino)piperidi... (S)-3-N-Cbz-AMINO-PIPERIDINE Benzyl (S)-piperidin-3-ylcarbamate benzyl N-(piperidin-3-yl)carbaMate (S)-benzyl piperidin-3-ylcarbamate benzyl (3S)-piperidin-3-ylcarbamate Benzyl (3S)-piperidin-3-ylcarbamate benzyl N-[(3S)-piperidin-3-yl]carbaMate (3S)-3-[(Benzyloxycarbonyl)amino]piperidine N-(3S)-3-Piperidinylcarbamic acid phenylmethyl ester Carbamic acid, N-[(3S)-3-piperidinyl]-, phenylmethyl ester |
| CAS | 478646-33-2 |
| InChI | InChI=1/C13H18N2O2/c16-13(15-12-7-4-8-14-9-12)17-10-11-5-2-1-3-6-11/h1-3,5-6,12,14H,4,7-10H2,(H,15,16)/t12-/m0/s1 |
benzyl (3S)-piperidin-3-ylcarbamate - Physico-chemical Properties
| Molecular Formula | C13H18N2O2 |
| Molar Mass | 234.29 |
| Density | 1.13 |
| Boling Point | 396.3±41.0 °C(Predicted) |
| Flash Point | 193.5°C |
| Vapor Presure | 1.73E-06mmHg at 25°C |
| pKa | 12.16±0.20(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
| Refractive Index | 1.557 |
benzyl (3S)-piperidin-3-ylcarbamate - Risk and Safety
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37 - Wear suitable gloves. |
| HS Code | 29333990 |
benzyl (3S)-piperidin-3-ylcarbamate - Introduction
Benzyl (3S)-piperidin-3-ylcarbamate is an organic compound with the chemical formula C19H22N2O2. It is a white crystalline powder, soluble in some organic solvents, such as alcohols, esters and chlorinated hydrocarbons.
benzyl (3S)-piperidin-3-ylcarbamate has a variety of applications. It is often used as an intermediate in organic synthesis for the synthesis of biologically active natural products and drug molecules. It can also be used as a derivative of chiral catalysts for asymmetric catalytic reactions in organic synthesis.
Benzyl (3S)-piperidin-3-ylcarbamate can be prepared by reacting aminopiperidine with chloroformyl chloride, and then reacting with benzaldehyde to generate the compound. Benzyl (3S)-piperidin-3-ylcarbamate can be purified by crystallization to give pure product.
Regarding safety information, since benzyl (3S)-piperidin-3-ylcarbamate is an organic compound, conventional laboratory safety measures should be followed when using and handling. It may have an irritating effect on the eyes and skin, and care should be taken to avoid direct contact. At the same time, in the use of the process should ensure good ventilation, to avoid inhalation of its dust or dissolved liquid gas. If necessary, refer to the relevant safety data and operating instructions.
benzyl (3S)-piperidin-3-ylcarbamate has a variety of applications. It is often used as an intermediate in organic synthesis for the synthesis of biologically active natural products and drug molecules. It can also be used as a derivative of chiral catalysts for asymmetric catalytic reactions in organic synthesis.
Benzyl (3S)-piperidin-3-ylcarbamate can be prepared by reacting aminopiperidine with chloroformyl chloride, and then reacting with benzaldehyde to generate the compound. Benzyl (3S)-piperidin-3-ylcarbamate can be purified by crystallization to give pure product.
Regarding safety information, since benzyl (3S)-piperidin-3-ylcarbamate is an organic compound, conventional laboratory safety measures should be followed when using and handling. It may have an irritating effect on the eyes and skin, and care should be taken to avoid direct contact. At the same time, in the use of the process should ensure good ventilation, to avoid inhalation of its dust or dissolved liquid gas. If necessary, refer to the relevant safety data and operating instructions.
Last Update：2024-04-09 21:11:58
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CAS: 478646-33-2
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QQ: 3008007409
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CAS: 478646-33-2
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Email: 3008007409@qq.com
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