Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester - Names and Identifiers
Name | (R)-1-Benzyl-3-N-Boc-aminopiperidine
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Synonyms | (R)-1-Benzyl-3-N-Boc-aminopiperidine (R)-1-BENZYL-3-N-BOC-AMINOPIPERIDINE (R)-N-Benzyl-3-N-boc-aminopiperidine (S)-3-(BOC-AMINO)-1-BENZYL-PIPERIDINE (S)-tert-butyl 1-benzylpiperidin-3-ylcarbamate tert-Butyl [(3S)-1-benzylpiperidin-3-yl]carbamate tert-butyl N-[(3S)-1-benzylpiperidin-3-yl]carbaMate (R)-(1-BENZYL-PIPERIDIN-3-YL)-CARBAMIC ACID TERT-BUTYL ESTER Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester Carbamic acid, [(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester (9CI)
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CAS | 216854-24-9
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InChI | InChI=1/C17H26N2O2/c1-17(2,3)21-16(20)18-15-10-7-11-19(13-15)12-14-8-5-4-6-9-14/h4-6,8-9,15H,7,10-13H2,1-3H3,(H,18,20)/t15-/m0/s1 |
Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester - Physico-chemical Properties
Molecular Formula | C17H26N2O2
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Molar Mass | 290.4 |
Density | 1.07±0.1 g/cm3(Predicted) |
Boling Point | 400.9±34.0 °C(Predicted) |
Flash Point | 196.235°C |
Vapor Presure | 0mmHg at 25°C |
pKa | 12.31±0.20(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.542 |
Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester - Risk and Safety
Safety Description | 24/25 - Avoid contact with skin and eyes.
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HS Code | 29333990 |
Carbamic acid, N-[(3S)-1-(phenylmethyl)-3-piperidinyl]-, 1,1-dimethylethyl ester - Introduction
(R)-is an organic compound with the formula C16H24N2O2. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: Colorless or light yellow solid
-Solubility: Soluble in organic solvents such as chloroform and dichloromethane
-Melting point: About 50-55 degrees Celsius
-Optically active: It has optical activity and is a (R)-configuration.
Use:
-As an important organic synthesis intermediate, it can be used to synthesize various compounds.
-in drug synthesis, can be used for the synthesis of anti-tumor, anti-inflammatory drugs.
Method:
The preparation method of
(R)-is as follows:
First, react N-tert-butoxycarbonylaminopiperidine with benzyl bromide to obtain (R)-phosphonium.
Safety Information:
This compound should be handled in accordance with laboratory safety procedures.
-Avoid inhalation, ingestion or skin contact.
-Wear appropriate protective glasses, gloves and lab coat during operation.
-Store away from heat sources and open flames and away from direct sunlight.
-Comply with local regulations when disposing of waste.
Last Update:2024-04-09 21:01:54