Piperidine, 4-(1,1-dimethylethyl)- - Names and Identifiers
Piperidine, 4-(1,1-dimethylethyl)- - Physico-chemical Properties
Molecular Formula | C9H19N
|
Molar Mass | 141.25 |
Storage Condition | Room Temprature |
Piperidine, 4-(1,1-dimethylethyl)- - Introduction
4-tert-butylpiperidine is an organic compound with the chemical formula C12H21N. It is a colorless or light yellow liquid that appears as a light yellow solid at high temperatures. The following is a description of the nature, use, preparation and safety information of 4-tert-butylpiperidine:
Nature:
- 4-tert-butylpiperidine has a lower melting point and boiling point, and a lower density.
-Soluble in many organic solvents, such as alcohols, ethers and ketones.
-Stable in the air and not susceptible to moisture.
-is alkaline and can react with acid.
Use:
- 4-tert-butylpiperidine is commonly used as a catalyst and reagent in organic synthesis reactions.
-In drug synthesis, it can be used to form a biologically active molecular skeleton.
-can be used to synthesize pesticides and insecticides containing piperidine structure.
Preparation Method:
There are many preparation methods of-4-tert-butylpiperidine. The common way is to introduce a hydrogen bond donor and acceptor on the piperidine molecule to form a 4-tert-butyl substituent. This can be achieved by carrying out a substitution reaction on the piperidine molecule.
-During the preparation process, pay attention to the safety of the operating conditions and reaction equipment, and follow the relevant chemical use and handling specifications.
Safety Information:
- 4-tert-butylpiperidine may be irritating to the eyes and skin. After contact, rinse the affected area with plenty of water immediately, and seek medical help if necessary.
-Wear appropriate personal protective equipment such as safety glasses, gloves and laboratory coats during use and handling.
-Please store and handle the compound properly, and avoid contact with oxidants and strong acids to avoid dangerous reactions.
Last Update:2024-04-09 15:16:34