3-硝基-7-并环化合物
3-Nitro-7-azaindole
CAS: 23709-47-9
Molecular Formula: C7H5N3O2
3-硝基-7-并环化合物 - Names and Identifiers
| Name | 3-Nitro-7-azaindole |
| Synonyms | 3-Nitro-7-azaindole 3-NITRO-7-AZAINDOLE 3-Nitro-1H-pyrrolo[2,3-b]pyridin 3-Nitro-1H-pyrrolo[2,3-b]pyridine 3-nitro-1H-pyrrolo[2,3-b]pyridine 1H-Pyrrolo[2,3-b]pyridine, 3-nitro- 1H-pyrrolo[2,3-b]pyridine, 3-nitro- |
| CAS | 23709-47-9 |
| InChI | InChI=1/C7H5N3O2/c11-10(12)6-4-9-7-5(6)2-1-3-8-7/h1-4H,(H,8,9) |
3-硝基-7-并环化合物 - Physico-chemical Properties
| Molecular Formula | C7H5N3O2 |
| Molar Mass | 163.13 |
| Density | 1.58±0.1 g/cm3(Predicted) |
| Melting Point | >300 °C |
| Boling Point | 380.0±35.0 °C(Predicted) |
| Flash Point | 187.3°C |
| Vapor Presure | 8.03E-06mmHg at 25°C |
| pKa | 3.13±0.20(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.74 |
| MDL | MFCD08272225 |
3-硝基-7-并环化合物 - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R36 - Irritating to the eyes |
| Safety Description | 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. |
| UN IDs | UN 2811 6.1/PG 3 |
| WGK Germany | 3 |
| HS Code | 29339900 |
| Hazard Class | IRRITANT |
3-硝基-7-并环化合物 - Introduction
3-Nitro-7-azaindole is an organic compound with the chemical formula C7H5N3O2. Its appearance is yellow to orange crystals.
3-Nitro-7-azaindole has a wide range of applications in the fields of medicinal chemistry and pesticides. It can be used as an intermediate in the synthesis of biologically active compounds. The compound has a structure similar to that of indole compounds, and can find new useful compounds in drug research. In addition, 3-Nitro-7-azaindole can also be used as a raw material for pesticides to control pests in crops.
There are various methods for preparing 3-Nitro-7-azaindole. A common method is prepared by nitration under nitrogen using pyridine as the solvent. Specific reaction conditions may also involve other reagents and reaction conditions, such as nitric acid and acid catalysts. During the preparation process, attention should be paid to safe operation and avoid contact and inhalation of compounds.
3-Nitro-7-azaindole's safety information has not been publicly reported. However, since it is a chemical, it should be used in accordance with the relevant safety practices. Appropriate personal protective equipment should be used to avoid contact with skin, eyes and respiratory tract. At the same time, pay attention to fire and explosion prevention measures during operation and storage, and properly manage waste disposal. When using and handling the compound, the relevant regulations and regulations should be followed.
3-Nitro-7-azaindole has a wide range of applications in the fields of medicinal chemistry and pesticides. It can be used as an intermediate in the synthesis of biologically active compounds. The compound has a structure similar to that of indole compounds, and can find new useful compounds in drug research. In addition, 3-Nitro-7-azaindole can also be used as a raw material for pesticides to control pests in crops.
There are various methods for preparing 3-Nitro-7-azaindole. A common method is prepared by nitration under nitrogen using pyridine as the solvent. Specific reaction conditions may also involve other reagents and reaction conditions, such as nitric acid and acid catalysts. During the preparation process, attention should be paid to safe operation and avoid contact and inhalation of compounds.
3-Nitro-7-azaindole's safety information has not been publicly reported. However, since it is a chemical, it should be used in accordance with the relevant safety practices. Appropriate personal protective equipment should be used to avoid contact with skin, eyes and respiratory tract. At the same time, pay attention to fire and explosion prevention measures during operation and storage, and properly manage waste disposal. When using and handling the compound, the relevant regulations and regulations should be followed.
Last Update：2024-04-09 21:11:58
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View History
3-硝基-7-并环化合物
(R)-1-[(R)-2-(二叔丁基膦)二茂铁基]乙基二(2-甲基苯基)膦
乙酸亞砷酸銅
2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-oxo-, 1,1-diMethylethyl ester
3-[2-羟基乙基-(3-甲基苯基)氨基]丙腈
N-(4-(N-(4-(N-(5-甲基异噁唑-3-基)氨磺酰基)苯基)氨磺酰基)苯基)乙酰胺
吉非水解物前体(盐酸盐)
2-苯基-3-2-丙烯醛
2,4-二甲氧基苯甲胺
UV-curing corrosion resistant coating
(R)-1-[(R)-2-(二叔丁基膦)二茂铁基]乙基二(2-甲基苯基)膦
乙酸亞砷酸銅
2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-oxo-, 1,1-diMethylethyl ester
3-[2-羟基乙基-(3-甲基苯基)氨基]丙腈
N-(4-(N-(4-(N-(5-甲基异噁唑-3-基)氨磺酰基)苯基)氨磺酰基)苯基)乙酰胺
吉非水解物前体(盐酸盐)
2-苯基-3-2-丙烯醛
2,4-二甲氧基苯甲胺
UV-curing corrosion resistant coating