220003-47-4
3-chloroazetidine
CAS: 220003-47-4
Molecular Formula: C3H6ClN
220003-47-4 - Names and Identifiers
| Name | 3-chloroazetidine |
| Synonyms | 3-chloroazetidine 3-CHLOROAZETIDINE |
| CAS | 220003-47-4 |
| InChI | InChI=1/C3H6ClN/c4-3-1-5-2-3/h3,5H,1-2H2 |
220003-47-4 - Physico-chemical Properties
| Molecular Formula | C3H6ClN |
| Molar Mass | 91.54 |
| Density | 1.16g/cm3 |
| Boling Point | 125.6°C at 760 mmHg |
| Flash Point | 29.8°C |
| Vapor Presure | 12.1mmHg at 25°C |
| Refractive Index | 1.48 |
220003-47-4 - Introduction
3-chloroazetidine(3-chloroazetidine) is an organic compound with the chemical formula C3H6ClN. It is a four-membered ring compound containing a Nitrogen heterocycle, in which a chlorine atom is substituted on one of the carbon atoms. The following is a description of the nature, use, preparation and safety information of 3-chloroazetidine:
Nature:
-Appearance: 3-chloroazetidine is a colorless or pale yellow liquid.
-Melting point:-35 ° C
-Boiling point: 115-116 ° C
-Density: approx. 1.109 g/mL
-Solubility: 3-chloroazetidine is soluble in many organic solvents, such as methanol, ether and dimethyl sulfoxide.
Use:
-Chemical synthesis: 3-chloroazetidine can be used as an intermediate in organic synthesis for the synthesis of biologically active compounds.
-Pharmaceutical manufacturing: It can be used to synthesize drugs, pesticides and other biologically active molecules.
-Surfactant: As a surfactant, 3-chloroazetidine can be used as a dye dispersant and wetting agent.
Method:
3-chloroazetidine can be prepared by the following methods:
-The chlorination reaction is carried out from 1,3-azetidine (1,3-azetidine) in the presence of a chlorinating agent (such as hydrogen chloride).
-3-chloroazetidine is obtained by reaction with sulfuryl chloride and ammonia.
Safety Information:
-Limited information is available on the toxicity and safety of 3-chloroazetidine. When using and handling this compound, it is recommended to follow laboratory safety practices, including wearing appropriate protective equipment.
-This compound needs to be stored in a cool, dry, well-ventilated place, away from flammable materials and oxidants.
-Eye, skin and respiratory tract irritation may result from exposure to 3-chloroazetidine. Personal protective equipment such as glasses, gloves and respiratory protection should be used if necessary.
-If ingested or inhaled 3-chloroazetidine, seek medical help immediately and provide detailed compound information.
Nature:
-Appearance: 3-chloroazetidine is a colorless or pale yellow liquid.
-Melting point:-35 ° C
-Boiling point: 115-116 ° C
-Density: approx. 1.109 g/mL
-Solubility: 3-chloroazetidine is soluble in many organic solvents, such as methanol, ether and dimethyl sulfoxide.
Use:
-Chemical synthesis: 3-chloroazetidine can be used as an intermediate in organic synthesis for the synthesis of biologically active compounds.
-Pharmaceutical manufacturing: It can be used to synthesize drugs, pesticides and other biologically active molecules.
-Surfactant: As a surfactant, 3-chloroazetidine can be used as a dye dispersant and wetting agent.
Method:
3-chloroazetidine can be prepared by the following methods:
-The chlorination reaction is carried out from 1,3-azetidine (1,3-azetidine) in the presence of a chlorinating agent (such as hydrogen chloride).
-3-chloroazetidine is obtained by reaction with sulfuryl chloride and ammonia.
Safety Information:
-Limited information is available on the toxicity and safety of 3-chloroazetidine. When using and handling this compound, it is recommended to follow laboratory safety practices, including wearing appropriate protective equipment.
-This compound needs to be stored in a cool, dry, well-ventilated place, away from flammable materials and oxidants.
-Eye, skin and respiratory tract irritation may result from exposure to 3-chloroazetidine. Personal protective equipment such as glasses, gloves and respiratory protection should be used if necessary.
-If ingested or inhaled 3-chloroazetidine, seek medical help immediately and provide detailed compound information.
Last Update：2024-04-09 15:17:55
