(R)-1-Cbz-3-(Boc-aMino)piperidine

(R)-1-Cbz-3-(Boc-aMino)piperidine - Names and Identifiers

Name	(R)-3-N-Boc-AMINO-1-Cbz-PIPERIDINE
Synonyms	(R)-1-Cbz-3-N-Boc-aMinopiperidine (R)-1-Cbz-3-(Boc-aMino)piperidine (R)-3-N-Boc-AMINO-1-Cbz-PIPERIDINE (R)-3-N-BOC-AMINO-1-CBZ-PIPERIDINE (R)-Benzyl 3-((Tert-Butoxycarbonyl)Amino)Piperidine-1-Carboxylate Benzyl (R)-3-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate benzyl (3r)-3-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate Benzyl (3R)-3-[(tert-butoxycarbonyl)amino]piperidine-1-carboxylate (3R)-3-[[(1,1-Dimethylethoxy)carbonyl]amino]-1-piperidinecarboxylic acid phenylmethyl ester (3r)-3-(((1,1-dimethylethoxy)carbonyl)amino)-1-piperidinecarboxylic acid phenylmethyl ester (3R)-3-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-1-piperidinecarboxylic acid (phenylmethyl) ester
CAS	485820-12-0

(R)-1-Cbz-3-(Boc-aMino)piperidine - Physico-chemical Properties

Molecular Formula	C18H26N2O4
Molar Mass	334.41
Density	1.15
Boling Point	471.9±44.0 °C(Predicted)
pKa	12.25±0.20(Predicted)
Storage Condition	2-8°C

(R)-1-Cbz-3-(Boc-aMino)piperidine - 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

(R)-1-Cbz-3-(Boc-aMino)piperidine - Introduction

(R)-I is an organic compound with the chemical name (R)-I.

Nature:
(R)-It is a colorless to pale yellow solid with a molecular formula of C22H32N2O3. It has a double bond, aromatic and aliphatic and other multiple bond structure. It has good stability at room temperature.

Use:
(R)-Often used as an intermediate in organic synthesis. It can be used to synthesize organic compounds such as peptides and drug molecules. It has good stereoselectivity and catalytic properties, and has a wide range of applications in the field of medicine.

Preparation Method: The preparation of
(R)-is usually carried out by organic synthesis methods. A common preparation method is to use aminopiperidine and N-tert-butoxycarbonyl-aminobenzoic acid benzyl ester as raw materials, through the appropriate solvent and catalyst, under certain conditions for reaction synthesis.

Safety Information:
(R)-is a chemical reagent that requires appropriate safety measures during handling and storage. It may be irritating to the skin and eyes. Appropriate personal protective equipment, such as lab gloves, protective glasses and laboratory coats, should be worn during use. In case of accidental contact with skin or eyes, rinse immediately with plenty of water. In addition, it should be kept away from fire and flammable materials, and stored in a cool, well-ventilated place. If necessary, professional personnel can be invited for handling and disposal. During use, please abide by relevant safety operation procedures and regulations.

Last Update：2024-04-09 02:00:46