3-TRIFLUOROMETHYL-P-TOLUIC ACID - Names and Identifiers
3-TRIFLUOROMETHYL-P-TOLUIC ACID - Physico-chemical Properties
Molecular Formula | C9H7F3O2
|
Molar Mass | 204.15 |
Density | 1.345±0.06 g/cm3(Predicted) |
Melting Point | 182-186°C |
Boling Point | 268.6±40.0 °C(Predicted) |
Flash Point | 94.7°C |
Solubility | soluble in Methanol |
Vapor Presure | 0.0573mmHg at 25°C |
Appearance | powder to crystal |
Color | White to Almost white |
pKa | 3.94±0.10(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.463 |
MDL | MFCD01631592 |
3-TRIFLUOROMETHYL-P-TOLUIC ACID - Risk and Safety
Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin.
R26/27/28 - Very toxic by inhalation, in contact with skin and if swallowed.
R36 - Irritating to the eyes
R22 - Harmful if swallowed
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
S24/25 - Avoid contact with skin and eyes.
S37 - Wear suitable gloves.
|
HS Code | 29163100 |
Hazard Class | IRRITANT |
3-TRIFLUOROMETHYL-P-TOLUIC ACID - Introduction
4-Methyl-3-(trifluoromethyl)benzoic acid, chemical formula C9H7F3O2, is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: White crystalline solid
-Molecular weight: 214.15g/mol
-Melting Point: 142-145 ° C
-Boiling point: 302 ° C
-Solubility: Soluble in organic solvents such as ethanol, ether and ether, insoluble in water.
-vulnerable to light, heat and moisture, to avoid exposure to light.
Use:
4-Methyl-3-(trifluoromethyl)benzoic acid is mainly used as catalyst and intermediate in organic synthesis:
-Catalyst: It can be used as a ligand of palladium catalyst and play a catalytic role in some chemical reactions.
-Intermediate: It can also be used as an intermediate in organic synthesis for the synthesis of other compounds.
Method:
4-Methyl-3-(trifluoromethyl)benzoic acid is usually synthesized by the following steps:
1. First, methylbenzaldehyde reacts with a trifluoromethyl acylating reagent to generate 3-trifluoromethyl-4-methylbenzaldehyde.
2.3-trifluoromethyl-4-methylbenzaldehyde is then reacted with sodium hydroxide to form sodium 4-Methyl-3-(trifluoromethyl)benzoic acid.
3. Finally, the resulting sodium salt reacts with an acid to produce 4-Methyl-3-(trifluoromethyl)benzoic acid.
Safety Information:
- 4-Methyl-3-(trifluoromethyl)benzoic acid can cause irritation to the eyes, skin and respiratory system.
-When using, pay attention to avoid inhalation, contact with skin and eyes, and wear protective equipment when necessary.
-In case of accidental contact, rinse the affected area with water immediately and seek medical help when needed.
-Store in a dry, cool place, away from fire and oxidizing agents.
Last Update:2024-04-10 22:29:15