4-(2-Ethylphenoxy)-3-fluoroaniline
4-(2-Ethylphenoxy)-3-fluoroaniline
CAS: 946664-00-2
Molecular Formula: C14H14FNO
4-(2-Ethylphenoxy)-3-fluoroaniline - Names and Identifiers
| Name | 4-(2-Ethylphenoxy)-3-fluoroaniline |
| Synonyms | 4-(2-ETHYLPHENOXY)-3-FLUOROANILINE 4-(2-Ethylphenoxy)-3-fluoroaniline |
| CAS | 946664-00-2 |
4-(2-Ethylphenoxy)-3-fluoroaniline - Physico-chemical Properties
| Molecular Formula | C14H14FNO |
| Molar Mass | 231.27 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD08687767 |
4-(2-Ethylphenoxy)-3-fluoroaniline - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Class | IRRITANT |
4-(2-Ethylphenoxy)-3-fluoroaniline - Introduction
4-(2-Ethylphenoxy)-3-fluoroaniline (4-(2-ethylphenoxy)-3-fluoroaniline) is an organic compound with the chemical formula C14H14FNO. It is a pale yellow to brown crystal or powder.
This compound is commonly used as an intermediate for glyphosate, a widely used herbicide. 4-(2-Ethylphenoxy)-3-fluoroaniline can also be used as dyes, fungicides and pharmaceutical intermediates. It has strong molecular polarity and glyphosate reactivity.
The method for preparing 4-(2-Ethylphenoxy)-3-fluoroaniline is usually synthesized by a substitution reaction between reagents. One common method is the condensation reaction of 2-ethylphenol and 3-fluoroaniline under basic or acidic conditions.
For safety information, 4-(2-Ethylphenoxy)-3-fluoroaniline may be acutely toxic and irritant, so appropriate personal protective measures, such as gloves, goggles and appropriate protective clothing, should be taken when using or handling this compound. In addition, the compound should be stored in a dry, well-ventilated place, away from fire and high temperature. It is necessary to operate and handle in strict accordance with the safety operation guidelines. Direct contact with the skin, eyes and mouth should be avoided in handling the compound. If accidental exposure or poisoning occurs, seek medical attention immediately.
This compound is commonly used as an intermediate for glyphosate, a widely used herbicide. 4-(2-Ethylphenoxy)-3-fluoroaniline can also be used as dyes, fungicides and pharmaceutical intermediates. It has strong molecular polarity and glyphosate reactivity.
The method for preparing 4-(2-Ethylphenoxy)-3-fluoroaniline is usually synthesized by a substitution reaction between reagents. One common method is the condensation reaction of 2-ethylphenol and 3-fluoroaniline under basic or acidic conditions.
For safety information, 4-(2-Ethylphenoxy)-3-fluoroaniline may be acutely toxic and irritant, so appropriate personal protective measures, such as gloves, goggles and appropriate protective clothing, should be taken when using or handling this compound. In addition, the compound should be stored in a dry, well-ventilated place, away from fire and high temperature. It is necessary to operate and handle in strict accordance with the safety operation guidelines. Direct contact with the skin, eyes and mouth should be avoided in handling the compound. If accidental exposure or poisoning occurs, seek medical attention immediately.
Last Update：2024-04-09 20:52:54
