(5E)-2-mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one
(5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one
CAS: 101444-70-6
Molecular Formula: C17H14N2O2S
(5E)-2-mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one - Names and Identifiers
(5E)-2-mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one - Physico-chemical Properties
| Molecular Formula | C17H14N2O2S |
| Molar Mass | 310.37 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD01848498 |
(5E)-2-mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one - Risk and Safety
| Hazard Class | IRRITANT |
(5E)-2-mercapto-5-(4-methoxybenzylidene)-3-phenyl-3,5-dihydro-4H-imidazol-4-one - Introduction
(5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3 is an organic compound whose chemical structure contains an imidazole ring and an alkene bond. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: Common for yellow to orange crystals
-Solubility: Good solubility in organic solvents, such as ether, dichloromethane, etc.
-Melting point: usually 80-85 ℃
Use:
- (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, frequently used as an intermediate in the synthesis of chemicals. Because of its structure containing imidazole ring and olefin bond, it can participate in a variety of organic synthesis reactions, and can be used to synthesize biologically active compounds.
Preparation Method:
-Generally, the preparation of (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, Al can be completed through a multi-step reaction. One common method of preparation is to proceed from appropriate starting materials through successive chemical conversion steps, ultimately leading to the desired product.
Safety Information:
- (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, no definitive safety data are currently available. However, as an organic compound, it may produce certain toxicity and irritation to human body. During handling and handling, proper laboratory safety procedures should be followed, and appropriate personal protective equipment such as laboratory gloves, goggles and protective clothing should be provided.
Nature:
-Appearance: Common for yellow to orange crystals
-Solubility: Good solubility in organic solvents, such as ether, dichloromethane, etc.
-Melting point: usually 80-85 ℃
Use:
- (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, frequently used as an intermediate in the synthesis of chemicals. Because of its structure containing imidazole ring and olefin bond, it can participate in a variety of organic synthesis reactions, and can be used to synthesize biologically active compounds.
Preparation Method:
-Generally, the preparation of (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, Al can be completed through a multi-step reaction. One common method of preparation is to proceed from appropriate starting materials through successive chemical conversion steps, ultimately leading to the desired product.
Safety Information:
- (5E)-2-Mercapto-5-(4-methoxybenzylidene)-3-phenyl-3, no definitive safety data are currently available. However, as an organic compound, it may produce certain toxicity and irritation to human body. During handling and handling, proper laboratory safety procedures should be followed, and appropriate personal protective equipment such as laboratory gloves, goggles and protective clothing should be provided.
Last Update：2024-04-09 21:04:16
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