2-(Hydroxymethyl)-5-(trifluoromethoxy)toluene, 4-(Hydroxymethyl)-3-methyl-alpha,alpha,alpha-trifluoroanisole
[2-Methyl-4-(trifluoromethoxy)phenyl]methanol
CAS: 261951-94-4
Molecular Formula: C9H9F3O2
2-(Hydroxymethyl)-5-(trifluoromethoxy)toluene, 4-(Hydroxymethyl)-3-methyl-alpha,alpha,alpha-trifluoroanisole - Names and Identifiers
2-(Hydroxymethyl)-5-(trifluoromethoxy)toluene, 4-(Hydroxymethyl)-3-methyl-alpha,alpha,alpha-trifluoroanisole - Physico-chemical Properties
| Molecular Formula | C9H9F3O2 |
| Molar Mass | 206.16 |
| Density | 1.289±0.06 g/cm3(Predicted) |
| Boling Point | 231.3±35.0 °C(Predicted) |
| pKa | 14.15±0.10(Predicted) |
| Sensitive | Irritant |
| MDL | MFCD01631546 |
2-(Hydroxymethyl)-5-(trifluoromethoxy)toluene, 4-(Hydroxymethyl)-3-methyl-alpha,alpha,alpha-trifluoroanisole - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Hazard Note | Irritant |
2-(Hydroxymethyl)-5-(trifluoromethoxy)toluene, 4-(Hydroxymethyl)-3-methyl-alpha,alpha,alpha-trifluoroanisole - Introduction
[2-Methyl-4-(trifluoromethoxy)phenyl]methanol is an organic compound with the chemical formula C10H11F3O2. It is a white solid with a carbinol structure with a phenyl group.
The following is an introduction to several aspects of the [2-Methyl-4-(trifluoromethoxy)phenyl]methanol:
1. nature:
-Appearance: White solid
-melting point: 64-68 ℃
-Boiling point: 224-226 ℃
-Solubility: Soluble in alcohol and ether, insoluble in water
2. use:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol is an important intermediate in organic synthesis, commonly used in the synthesis of pesticides, pharmaceuticals and dyes and other compounds. Its fluorine-containing group can enhance the stability and biological activity of the compound.
3. preparation method:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol is usually prepared by reacting benzyl benzoate with trifluoromethyl alcohol. The specific reaction conditions can be adjusted according to the experimental needs.
4. Safety Information:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol may be irritating to eyes and skin, so you should pay attention to protective measures to avoid contact with skin and eyes.
-When storing and handling, keep away from ignition and oxidizing agents.
-When using and handling, be careful to avoid inhalation or ingestion, and wear appropriate protective equipment, such as gloves, safety glasses and protective masks, if necessary.
Please note that the use and operation of chemicals should follow safe operating procedures and be carried out under suitable facilities to ensure personal safety and the success of the experiment.
The following is an introduction to several aspects of the [2-Methyl-4-(trifluoromethoxy)phenyl]methanol:
1. nature:
-Appearance: White solid
-melting point: 64-68 ℃
-Boiling point: 224-226 ℃
-Solubility: Soluble in alcohol and ether, insoluble in water
2. use:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol is an important intermediate in organic synthesis, commonly used in the synthesis of pesticides, pharmaceuticals and dyes and other compounds. Its fluorine-containing group can enhance the stability and biological activity of the compound.
3. preparation method:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol is usually prepared by reacting benzyl benzoate with trifluoromethyl alcohol. The specific reaction conditions can be adjusted according to the experimental needs.
4. Safety Information:
- [2-Methyl-4-(trifluoromethoxy)phenyl]methanol may be irritating to eyes and skin, so you should pay attention to protective measures to avoid contact with skin and eyes.
-When storing and handling, keep away from ignition and oxidizing agents.
-When using and handling, be careful to avoid inhalation or ingestion, and wear appropriate protective equipment, such as gloves, safety glasses and protective masks, if necessary.
Please note that the use and operation of chemicals should follow safe operating procedures and be carried out under suitable facilities to ensure personal safety and the success of the experiment.
Last Update：2024-04-09 20:44:15
Supplier List
View History