Benzonitrile, 2,4,5-trifluoro-3-methoxy-6-methyl-
2,4,5-Trifluoro-3-methoxy-6-methylbenzonitrile
CAS: 1003708-50-6
Molecular Formula: C9H6F3NO
Benzonitrile, 2,4,5-trifluoro-3-methoxy-6-methyl- - Names and Identifiers
| Name | 2,4,5-Trifluoro-3-methoxy-6-methylbenzonitrile |
| Synonyms | 3-Methoxy-2,4,5-trifluoromethylbenzonitrile 3-METHOXY -2,4,5-TRIFLUOROMETHYLBENZONITRILE 2,4,5-Trifluoro-3-methoxy-6-methylbenzonitrile Benzonitrile, 2,4,5-trifluoro-3-methoxy-6-methyl- |
| CAS | 1003708-50-6 |
| InChI | InChI=1S/C9H6F3NO/c1-4-5(3-13)7(11)9(14-2)8(12)6(4)10/h1-2H3 |
Benzonitrile, 2,4,5-trifluoro-3-methoxy-6-methyl- - Physico-chemical Properties
| Molecular Formula | C9H6F3NO |
| Molar Mass | 201.15 |
| Density | 1.31±0.1 g/cm3(Predicted) |
| Boling Point | 242.9±40.0 °C(Predicted) |
Benzonitrile, 2,4,5-trifluoro-3-methoxy-6-methyl- - Introduction
3-Methoxy-2, 4,5-trifluoromethylbenzonitrile is an organic compound. Its chemical formula is C9H6F3NO and its molecular weight is 191.14g/mol.
Nature:
1. Appearance: colorless or yellowish solid;
2. melting point: 64-67 ℃;
3. boiling point: 187-189 ℃;
4. Solubility: Soluble in organic solvents, such as ethers, alcohols and ketones;
5. stability: stable at room temperature.
Use:
3-methoxy-2, 4,5-trifluoromethyl benzonitrile can be used as an effective pesticide intermediate, mainly for the synthesis of various heterocyclopesticides. It has good bactericidal and insecticidal activity, and has a wide range of applications in the field of agriculture.
Preparation Method:
The synthesis of 3-methoxy-2, 4,5-trifluoromethyl benzonitrile is generally obtained by reacting benzonitrile with methoxylating reagents (such as methyl iodide and sodium methane, etc.). The specific steps can be adjusted according to the experimental conditions and reaction requirements.
Safety Information:
1.3-Methoxy-2, 4,5-trifluoromethylbenzonitrile is an organic compound, which has certain toxicity and should be operated in accordance with safe operation regulations;
2. During use, direct contact with skin and eyes should be avoided. If contact is not careful, rinse with plenty of water and seek medical treatment in time;
3. should be placed in a cool, dry place, away from fire and heat;
4. in handling, storage and use, attention should be paid to prevent contact with strong oxidants, strong acids and other substances to avoid dangerous reactions.
The above is only a brief introduction. For specific operation and safety measures, please refer to relevant literature and laboratory guidance in practical application.
Nature:
1. Appearance: colorless or yellowish solid;
2. melting point: 64-67 ℃;
3. boiling point: 187-189 ℃;
4. Solubility: Soluble in organic solvents, such as ethers, alcohols and ketones;
5. stability: stable at room temperature.
Use:
3-methoxy-2, 4,5-trifluoromethyl benzonitrile can be used as an effective pesticide intermediate, mainly for the synthesis of various heterocyclopesticides. It has good bactericidal and insecticidal activity, and has a wide range of applications in the field of agriculture.
Preparation Method:
The synthesis of 3-methoxy-2, 4,5-trifluoromethyl benzonitrile is generally obtained by reacting benzonitrile with methoxylating reagents (such as methyl iodide and sodium methane, etc.). The specific steps can be adjusted according to the experimental conditions and reaction requirements.
Safety Information:
1.3-Methoxy-2, 4,5-trifluoromethylbenzonitrile is an organic compound, which has certain toxicity and should be operated in accordance with safe operation regulations;
2. During use, direct contact with skin and eyes should be avoided. If contact is not careful, rinse with plenty of water and seek medical treatment in time;
3. should be placed in a cool, dry place, away from fire and heat;
4. in handling, storage and use, attention should be paid to prevent contact with strong oxidants, strong acids and other substances to avoid dangerous reactions.
The above is only a brief introduction. For specific operation and safety measures, please refer to relevant literature and laboratory guidance in practical application.
Last Update：2024-04-10 22:29:15
