(3,4-diaminophenyl)(4-fluorophenyl)methanone
(3,4-diaminophenyl) (4-fluorophenyl) ketone
CAS: 66938-86-1
Molecular Formula: C13H11FN2O
(3,4-diaminophenyl)(4-fluorophenyl)methanone - Names and Identifiers
| Name | (3,4-diaminophenyl) (4-fluorophenyl) ketone |
| Synonyms | (3,4-diaminophenyl) (4-fluorophenyl) ketone (3,4-diaminophenyl)(4-fluorophenyl)methanone (3,4-Diaminophenyl)(4-Fluoro Phenyl)Methanone (3,4-DIAMINOPHENYL)(4-FLUORO PHENYL)METHANONE Methanone, (3,4-diaminophenyl)(4-fluorophenyl)- |
| CAS | 66938-86-1 |
| EINECS | 266-522-8 |
| InChI | InChI=1/C13H11FN2O/c14-10-4-1-8(2-5-10)13(17)9-3-6-11(15)12(16)7-9/h1-7H,15-16H2 |
(3,4-diaminophenyl)(4-fluorophenyl)methanone - Physico-chemical Properties
| Molecular Formula | C13H11FN2O |
| Molar Mass | 230.24 |
| Density | 1.305±0.06 g/cm3 (20 ºC 760 Torr) |
| Melting Point | 113-114℃ (methanol ) |
| Boling Point | 447.4±45.0 °C(Predicted) |
| Flash Point | 224.4°C |
| Vapor Presure | 3.38E-08mmHg at 25°C |
| pKa | 2.76±0.10(Predicted) |
| Refractive Index | 1.652 |
(3,4-diaminophenyl)(4-fluorophenyl)methanone - Introduction
(3,4-diaminophenyl) (4-fluorophenyl) ketone is an organic compound whose chemical structure contains a (3,4-diaminophenyl) group and a (4-fluorophenyl) group, as well as a methanone functional group. It has a molecular formula of C13H11FNO and a molecular weight of 225.23g/mol.
(3,4-diaminophenyl) (4-fluorophenyl) ketone's properties are mainly manifested in its chemical reaction and physical properties. The compound is a colorless crystalline solid at room temperature and is flammable. It is insoluble in water, but soluble in many organic solvents such as ethanol and dimethylformamide.
(3,4-diaminophenyl) (4-fluorophenyl) ketone has certain application value in chemical research and synthesis. It can be used as an intermediate or starting material in organic synthesis reactions. For example, it can play an important role in the synthesis of aromatic compounds or drug molecules.
The preparation of this compound generally adopts the method of organic synthesis. A common synthetic method is to react (3,4-diaminophenyl) (4-fluorophenyl) amine with acetone to obtain the target product by amination of the ortho amino group of aromatic ketone.
Regarding the safety information of (3,4-diaminophenyl) (4-fluorophenyl) ketone, due to its flammability and possible irritation to skin and eyes, protective gloves, goggles and protective clothing should be worn during operation. In addition, the toxicity and environmental impact of the compound still need to be further studied and evaluated. When using or handling, please follow the chemical safety practice and relevant regulations.
(3,4-diaminophenyl) (4-fluorophenyl) ketone's properties are mainly manifested in its chemical reaction and physical properties. The compound is a colorless crystalline solid at room temperature and is flammable. It is insoluble in water, but soluble in many organic solvents such as ethanol and dimethylformamide.
(3,4-diaminophenyl) (4-fluorophenyl) ketone has certain application value in chemical research and synthesis. It can be used as an intermediate or starting material in organic synthesis reactions. For example, it can play an important role in the synthesis of aromatic compounds or drug molecules.
The preparation of this compound generally adopts the method of organic synthesis. A common synthetic method is to react (3,4-diaminophenyl) (4-fluorophenyl) amine with acetone to obtain the target product by amination of the ortho amino group of aromatic ketone.
Regarding the safety information of (3,4-diaminophenyl) (4-fluorophenyl) ketone, due to its flammability and possible irritation to skin and eyes, protective gloves, goggles and protective clothing should be worn during operation. In addition, the toxicity and environmental impact of the compound still need to be further studied and evaluated. When using or handling, please follow the chemical safety practice and relevant regulations.
Last Update：2024-04-09 21:54:55
