(E)-4-Amino-1,1,1-trifluoro-but-3-en-2-one
4-Amino-1,1,1-trifluoro-3-buten-2-one
CAS: 184848-89-3
Molecular Formula: C4H4F3NO
(E)-4-Amino-1,1,1-trifluoro-but-3-en-2-one - Names and Identifiers
(E)-4-Amino-1,1,1-trifluoro-but-3-en-2-one - Physico-chemical Properties
| Molecular Formula | C4H4F3NO |
| Molar Mass | 139.08 |
| Density | 1.319±0.06 g/cm3(Predicted) |
| Boling Point | 95.3±40.0 °C(Predicted) |
| Flash Point | 11.421°C |
| Vapor Presure | 45.759mmHg at 25°C |
| pKa | 4.94±0.70(Predicted) |
| Storage Condition | 2-8℃ |
| Refractive Index | 1.384 |
(E)-4-Amino-1,1,1-trifluoro-but-3-en-2-one - Introduction
4-Amino-1,1,1-trifluoro-3-buten-2-one, chemical formula C4H5F3NO, also known as AFP in the field of chemistry. The following is an introduction to the nature, use, formulation and safety information of AFP:
Nature:
- AFP is a colorless to pale yellow liquid with a pungent odor.
-It has a lower boiling point and melting point, can be evaporated at room temperature, and is easy to volatilize.
- AFP has strong activity and can be used as a reagent of alkylene oxide to perform ring opening and closing reactions with heterocyclic compounds.
-It is stable under acidic conditions, but may decompose under alkaline conditions.
Use:
- AFP is widely used as an important reagent in the field of organic synthesis for the synthesis of various organic compounds.
-It can be used to synthesize organic compounds such as drugs, dyes, spices and pesticides.
Method:
The preparation of AFP is usually achieved by the reaction of trifluoroacetone and N-butylamine. First, under alkaline conditions, n-butylamine reacts with trifluoroacetone to generate AFP, and then the pure product is obtained from the reaction mixture through crystallization and other processes.
Safety Information:
- AFP is an organic compound, contact or inhalation of AFP may be harmful to the human body.
-It is an irritating compound that may cause irritation to the eyes, skin and respiratory system.
-observe appropriate safety measures when using AFP, such as wearing protective gloves, glasses and respiratory protection.
-when using or storing AFP, avoid contact with oxidants, strong acids and strong bases.
Please note that AFP is a chemical substance and should be used with caution, and the relevant safety instructions and operating procedures should be carefully read and followed before using the compound.
Nature:
- AFP is a colorless to pale yellow liquid with a pungent odor.
-It has a lower boiling point and melting point, can be evaporated at room temperature, and is easy to volatilize.
- AFP has strong activity and can be used as a reagent of alkylene oxide to perform ring opening and closing reactions with heterocyclic compounds.
-It is stable under acidic conditions, but may decompose under alkaline conditions.
Use:
- AFP is widely used as an important reagent in the field of organic synthesis for the synthesis of various organic compounds.
-It can be used to synthesize organic compounds such as drugs, dyes, spices and pesticides.
Method:
The preparation of AFP is usually achieved by the reaction of trifluoroacetone and N-butylamine. First, under alkaline conditions, n-butylamine reacts with trifluoroacetone to generate AFP, and then the pure product is obtained from the reaction mixture through crystallization and other processes.
Safety Information:
- AFP is an organic compound, contact or inhalation of AFP may be harmful to the human body.
-It is an irritating compound that may cause irritation to the eyes, skin and respiratory system.
-observe appropriate safety measures when using AFP, such as wearing protective gloves, glasses and respiratory protection.
-when using or storing AFP, avoid contact with oxidants, strong acids and strong bases.
Please note that AFP is a chemical substance and should be used with caution, and the relevant safety instructions and operating procedures should be carefully read and followed before using the compound.
Last Update：2024-04-09 21:01:54
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