6-amidinoindole
1H-indole-6-carboximidamide
CAS: 71889-72-0
Molecular Formula: C9H9N3
6-amidinoindole - Names and Identifiers
| Name | 1H-indole-6-carboximidamide |
| Synonyms | 6-amidinoindole 1H-indole-6-carboximidamide 1H-Indole-6-carboxiMidaMide |
| CAS | 71889-72-0 |
| InChI | InChI=1/C9H9N3/c10-9(11)7-2-1-6-3-4-12-8(6)5-7/h1-5,12H,(H3,10,11) |
6-amidinoindole - Physico-chemical Properties
| Molecular Formula | C9H9N3 |
| Molar Mass | 159.19 |
| Density | 1.34±0.1 g/cm3(Predicted) |
| Boling Point | 364.6±34.0 °C(Predicted) |
| Flash Point | 174.3°C |
| Vapor Presure | 1.66E-05mmHg at 25°C |
| pKa | 16.05±0.30(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
| Refractive Index | 1.699 |
6-amidinoindole - Introduction
1H-indole-6-carboximidamide(1H-indole-6-carboximidamide) is an organic compound with the chemical formula C9H9N3. It is a derivative of indole compounds.
Properties: 1H-indole-6-carboximidamide is a colorless crystal with a high melting point. It is sparingly soluble in water and soluble in organic solvents such as ethanol and dichloromethane. Its structure contains a pyrrole ring and an amino amidine functional group.
use: 1H-indole-6-carboximidamide has certain uses in the field of biomedicine. Studies have shown that it may have anti-inflammatory, antioxidant and anti-tumor activities. Therefore, it is widely used in drug research and development.
Preparation method: The preparation method of 1H-indole-6-carboximidamide is mainly obtained by reacting an appropriate precursor compound with aminoamidine. A common synthesis method is to react 1H-indole-6-carboxylic acid with amino amidine in an appropriate solvent, and then obtain the target product after appropriate purification treatment.
Safety information: At present, there are relatively few studies on the toxicity and safety of 1H-indole-6-carboximidamide, so its accurate safety information needs further research and evaluation. However, in general, care should be taken to avoid contact with skin and eyes during operation, and at the same time, it should be operated in a well-ventilated place. Appropriate protective measures should be used during use, such as wearing laboratory protective clothing, respiratory protection, etc.
Properties: 1H-indole-6-carboximidamide is a colorless crystal with a high melting point. It is sparingly soluble in water and soluble in organic solvents such as ethanol and dichloromethane. Its structure contains a pyrrole ring and an amino amidine functional group.
use: 1H-indole-6-carboximidamide has certain uses in the field of biomedicine. Studies have shown that it may have anti-inflammatory, antioxidant and anti-tumor activities. Therefore, it is widely used in drug research and development.
Preparation method: The preparation method of 1H-indole-6-carboximidamide is mainly obtained by reacting an appropriate precursor compound with aminoamidine. A common synthesis method is to react 1H-indole-6-carboxylic acid with amino amidine in an appropriate solvent, and then obtain the target product after appropriate purification treatment.
Safety information: At present, there are relatively few studies on the toxicity and safety of 1H-indole-6-carboximidamide, so its accurate safety information needs further research and evaluation. However, in general, care should be taken to avoid contact with skin and eyes during operation, and at the same time, it should be operated in a well-ventilated place. Appropriate protective measures should be used during use, such as wearing laboratory protective clothing, respiratory protection, etc.
Last Update：2024-04-09 20:49:11
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Mobile: 18021002903
QQ: 3008007409
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