3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester

3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester - Names and Identifiers

Name	3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester
Synonyms	Ethyl 3-(4'-Cbz)piperidine-3-aminopropionate 3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester benzyl 4-(1-amino-3-ethoxy-3-oxopropyl)piperidine-1-carboxylate Benzyl 4-(1-amino-3-ethoxy-3-oxopropyl)piperidine-1-carboxylate 4-Piperidinepropanoic acid, β-amino-1-[(phenylmethoxy)carbonyl]-, ethyl ester 4-Piperidinepropanoic acid, .beta.-amino-1-[(phenylmethoxy)carbonyl]-, ethyl ester
CAS	886362-29-4
InChI	InChI=1/C18H26N2O4/c1-2-23-17(21)12-16(19)15-8-10-20(11-9-15)18(22)24-13-14-6-4-3-5-7-14/h3-7,15-16H,2,8-13,19H2,1H3

3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester - Physico-chemical Properties

Molecular Formula	C18H26N2O4
Molar Mass	334.41
Density	1.16g/cm³
Boling Point	472.8°C at 760 mmHg
Flash Point	239.7°C
Vapor Presure	4.17E-09mmHg at 25°C
Storage Condition	2-8°C
Refractive Index	1.54

3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester - Introduction

3-Amino-3-(4 '-Cbz)piperidine-propionic acid ethyl ester is a compound with the chemical name 3-Amino-3-(4'-Cbz)piperidine-propionic acid ethyl ester.

Nature:
The compound is a solid with the appearance of yellowish or white crystals. It is almost insoluble in water at room temperature, but can be dissolved in common organic solvents, such as ethanol, dimethylformamide, etc.

Use:
This compound is a commonly used chemical reagent in organic synthesis, mainly for the synthesis of drugs, biological molecules and organic compounds. It can be introduced into other molecules as an important functional group to change its properties or increase its activity. In addition, it can also be used to synthesize various polymer materials and polymers.

Preparation Method:
3-Amino-3-(4 '-Cbz)piperidine-propionic acid ethyl ester can be synthesized by a variety of methods. A common preparation method is to react 4 '-piperidinecarboxylic acid with 3-aminopropanol, and then acylate the product obtained by the reaction to obtain the target compound.

Safety Information:
This compound is generally a safer compound under normal use conditions, but appropriate safety measures are still required. Avoid contact with skin and eyes to avoid irritation or injury. Wear appropriate protective gloves and glasses during operation. If accidental contact with skin or eyes, rinse immediately with plenty of water and seek medical help. The safety procedures of the laboratory should be observed when using the compound.

Last Update：2024-04-09 20:52:54