5339-74-2
4-hydroxybenzaldehyde thiosemicarbazone
CAS: 5339-74-2
Molecular Formula: C8H9N3OS
5339-74-2 - Names and Identifiers
| Name | 4-hydroxybenzaldehyde thiosemicarbazone |
| Synonyms | Nsc 3555 Ai3-18590 Brn 2097419 Einecs 226-273-8 4-hydroxybenzaldehyde thiosemicarbazone 1-(p-Hydroxybenzylidene)thiosemicarbazide Benzaldehyde, p-hydroxy-, thiosemicarbazone Hydrazinecarbothioamide, 2-[(4-hydroxyphenyl)methylene]- Hydrazinecarbothioamide, 2-((4-hydroxyphenyl)methylene)- (9ci) |
| CAS | 5339-74-2 |
| EINECS | 2262738 |
| InChI | InChI=1/C8H9N3OS/c9-8(13)11-10-5-6-1-3-7(12)4-2-6/h1-5,10H,(H3,9,11,13) |
5339-74-2 - Physico-chemical Properties
| Molecular Formula | C8H9N3OS |
| Molar Mass | 195.24 |
| Density | 1.2788 (rough estimate) |
| Boling Point | 351.2°C at 760 mmHg |
| Flash Point | 166.2°C |
| Vapor Presure | 4.17E-05mmHg at 25°C |
| Refractive Index | 1.7190 (estimate) |
5339-74-2 - Introduction
4-hydroxybenzaldehyde thiosemicarbazone(4-hydroxybenzaldehyde thiosemicarbazone) is an organic compound. The following is an introduction to some of its properties, uses, methods and safety information:
Nature:
-Appearance: The common form is white to light yellow crystalline powder.
-Solubility: It can be dissolved in water and some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
-Stability: It is relatively stable at room temperature.
Use:
-Chemical analysis: It is often used as a ligand for metal ions, especially complexing agents for metal ions such as nickel, copper, cobalt, and iron. This makes it have important applications in analytical chemistry.
-Drug research: It has a variety of biological activities, such as antibacterial and antiviral activities. Therefore, it is being investigated as a potential antibacterial and antiviral drug.
Preparation Method:
-It can be prepared by reacting 4-hydroxybenzene (methyl) aldehyde with thiosemicarbazone. The reaction is generally carried out in a suitable solvent under neutral or acidic conditions.
Safety Information:
-Since the toxicity of the compound has not been fully studied, caution is required during use and handling. Appropriate safety precautions should be taken to avoid contact with skin and eyes, and to avoid inhalation or ingestion of the compound.
-Wear appropriate protective gloves, glasses, and personal protective equipment such as lab coats when handling the compound to ensure a well-ventilated laboratory environment.
Nature:
-Appearance: The common form is white to light yellow crystalline powder.
-Solubility: It can be dissolved in water and some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
-Stability: It is relatively stable at room temperature.
Use:
-Chemical analysis: It is often used as a ligand for metal ions, especially complexing agents for metal ions such as nickel, copper, cobalt, and iron. This makes it have important applications in analytical chemistry.
-Drug research: It has a variety of biological activities, such as antibacterial and antiviral activities. Therefore, it is being investigated as a potential antibacterial and antiviral drug.
Preparation Method:
-It can be prepared by reacting 4-hydroxybenzene (methyl) aldehyde with thiosemicarbazone. The reaction is generally carried out in a suitable solvent under neutral or acidic conditions.
Safety Information:
-Since the toxicity of the compound has not been fully studied, caution is required during use and handling. Appropriate safety precautions should be taken to avoid contact with skin and eyes, and to avoid inhalation or ingestion of the compound.
-Wear appropriate protective gloves, glasses, and personal protective equipment such as lab coats when handling the compound to ensure a well-ventilated laboratory environment.
Last Update：2024-04-09 21:04:16
