5-fluoroindole-3-carboxaldehyde
5-fluoroindole-3-carboxaldehyde
CAS: 2338-71-8
Molecular Formula: C9H6FNO
5-fluoroindole-3-carboxaldehyde - Names and Identifiers
| Name | 5-fluoroindole-3-carboxaldehyde |
| Synonyms | AKOS JY2083653 TIMTEC-BB SBB002930 5-Fluoro-3-formylindole 5-FLUOROINDOLE-3-ALDEHYDE 5-FLUOROINDOLE-3-CARBALDEHYDE 5-FLUOROINDOLE-3-CARBOXALDEHYDE 5-fluoroindole-3-carboxaldehyde 5-fluoro-1H-indole-3-carbaldehyde 5-FLUORO-1H-INDOLE-3-CARBALDEHYDE 5-FLUORO-1H-INDOLE-3-CARBOXALDEHYDE |
| CAS | 2338-71-8 |
| InChI | InChI=1/C9H6FNO/c10-7-1-2-9-8(3-7)6(5-12)4-11-9/h1-5,11H |
5-fluoroindole-3-carboxaldehyde - Physico-chemical Properties
| Molecular Formula | C9H6FNO |
| Molar Mass | 163.15 |
| Density | 1.385±0.06 g/cm3(Predicted) |
| Melting Point | 164°C |
| Boling Point | 342.4±22.0 °C(Predicted) |
| Flash Point | 160.9°C |
| Vapor Presure | 7.53E-05mmHg at 25°C |
| Appearance | Solid |
| Color | yellow to green |
| BRN | 1449216 |
| pKa | 14.66±0.30(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
| Sensitive | Air Sensitive |
| Refractive Index | 1.695 |
| MDL | MFCD00022719 |
5-fluoroindole-3-carboxaldehyde - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
| HS Code | 29339900 |
| Hazard Class | IRRITANT |
5-fluoroindole-3-carboxaldehyde - Introduction
It is an organic compound with the chemical formula C9H6FNO. It has the appearance of a pale yellow solid.
Regarding the properties of this compound, there are the following points:
1. Melting Point: about 63-66 ℃.
2. Boiling point: About 286-288 ℃.
3. Solubility: It has high solubility in some organic solvents, such as dimethyl sulfoxide and dichloromethane.
4. Chemical reaction: It has an aldehyde functional group and can undergo typical aldehyde reactions, such as electrophilic addition, oxidation, etc.
There is not much research on the use of this compound, but it may be used as an intermediate in organic synthesis to prepare other organic compounds. Because of its structure containing fluorine atoms and indole nuclei, it may have potential applications in anti-tumor and other aspects.
Methods of Preparation:
A common preparation method is to start from the starting material of indole, first react indole with trifluorosuccinyl chloride (TFAA) to obtain trifluorosuccinyl indole (trifluoroacetate indole), the product is then reacted with hydrazine hydrate to remove the trifluoroacetyl group to obtain the calcium halide.
There is no detailed report on the safety information of this compound. Because it is an organic compound, it should generally be handled correctly in the laboratory and comply with relevant laboratory safety practices. The compound may have potential effects on the human body, so appropriate protective measures should be taken when using it, such as wearing protective glasses and gloves, and ensuring a well-ventilated laboratory environment. If it needs to be applied to commercial production or other specific scenarios, relevant safety assessment and control measures should be made according to the specific situation.
Regarding the properties of this compound, there are the following points:
1. Melting Point: about 63-66 ℃.
2. Boiling point: About 286-288 ℃.
3. Solubility: It has high solubility in some organic solvents, such as dimethyl sulfoxide and dichloromethane.
4. Chemical reaction: It has an aldehyde functional group and can undergo typical aldehyde reactions, such as electrophilic addition, oxidation, etc.
There is not much research on the use of this compound, but it may be used as an intermediate in organic synthesis to prepare other organic compounds. Because of its structure containing fluorine atoms and indole nuclei, it may have potential applications in anti-tumor and other aspects.
Methods of Preparation:
A common preparation method is to start from the starting material of indole, first react indole with trifluorosuccinyl chloride (TFAA) to obtain trifluorosuccinyl indole (trifluoroacetate indole), the product is then reacted with hydrazine hydrate to remove the trifluoroacetyl group to obtain the calcium halide.
There is no detailed report on the safety information of this compound. Because it is an organic compound, it should generally be handled correctly in the laboratory and comply with relevant laboratory safety practices. The compound may have potential effects on the human body, so appropriate protective measures should be taken when using it, such as wearing protective glasses and gloves, and ensuring a well-ventilated laboratory environment. If it needs to be applied to commercial production or other specific scenarios, relevant safety assessment and control measures should be made according to the specific situation.
Last Update：2024-04-10 22:29:15
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View History
5-fluoroindole-3-carboxaldehyde
2-溴-4-氟苯甲酸
氢溴酸右美沙芬
alpha-溴代对氯苯乙酸
5-Amino-6-nitroquinoline
N - CBZ - 4 - piperidine forMic acid
H-p-Chloro-D-Phe-OMe.HCl
3-溴-5-氯苯腈
1,1,3-trichloropropane
(1,1-Dimethylethyl)phenylphosphinous chloride
2-溴-4-氟苯甲酸
氢溴酸右美沙芬
alpha-溴代对氯苯乙酸
5-Amino-6-nitroquinoline
N - CBZ - 4 - piperidine forMic acid
H-p-Chloro-D-Phe-OMe.HCl
3-溴-5-氯苯腈
1,1,3-trichloropropane
(1,1-Dimethylethyl)phenylphosphinous chloride