Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)-
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride
CAS: 465513-98-8
Molecular Formula: C9 H5 Cl N2 O S
Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)- - Names and Identifiers
| Name | 4-(1,2,3-thiadiazol-4-yl)benzoyl chloride |
| Synonyms | 4-(1,2,3-THIADIAZOL-4-YL)BENZOYL CHLORIDE 4-(1,2,3-thiadiazol-4-yl)benzoyl chloride Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)- |
| CAS | 465513-98-8 |
| InChI | InChI=1/C9H5ClN2OS/c10-9(13)7-3-1-6(2-4-7)8-5-14-12-11-8/h1-5H |
Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)- - Physico-chemical Properties
| Molecular Formula | C9 H5 Cl N2 O S |
| Molar Mass | 224.67 |
| Density | 1.430±0.06 g/cm3(Predicted) |
| Melting Point | 168 °C |
| Boling Point | 368.8±44.0 °C(Predicted) |
| Flash Point | 176.9°C |
| Vapor Presure | 1.24E-05mmHg at 25°C |
| pKa | -4.97±0.34(Predicted) |
| Refractive Index | 1.626 |
Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)- - Risk and Safety
| Hazard Symbols | C - Corrosive |
| Risk Codes | R34 - Causes burns |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| HS Code | 29349990 |
Benzoyl chloride, 4-(1,2,3-thiadiazol-4-yl)- - Introduction
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is an organic compound with the chemical formula C9H5ClN2OS. The following is a description of the properties, uses, preparation and safety information of the compound:
1. nature:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is a colorless or pale yellow liquid with a pungent odor. It is an organic acid chloride compound with high reactivity. It can react with many nucleophiles, such as amines, alcohols, and active hydrogen-containing compounds.
2. use:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride has a wide range of applications in organic synthesis. It is an important intermediate for the preparation of compounds with biological activity. For example, it can be used to synthesize drugs, pesticides and other biologically active molecules. In addition, it can also be used to synthesize functional polymers and coating materials.
3. Preparation method:
The preparation method of 4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is generally obtained by reacting 4-(1,2,3-thiadiazol-4-yl) benzoic acid with astatine chloride or arsenic chloride under appropriate conditions. The specific reaction conditions can be adjusted according to actual needs.
4. Safety Information:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is an irritating compound and is corrosive. Wear appropriate protective equipment such as glasses, gloves, and lab coats when handling the compound. Avoid contact with skin and eyes. It should be operated in a well-ventilated place to avoid inhaling its vapors. If you come into contact with this compound, rinse immediately with plenty of water and seek medical help.
1. nature:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is a colorless or pale yellow liquid with a pungent odor. It is an organic acid chloride compound with high reactivity. It can react with many nucleophiles, such as amines, alcohols, and active hydrogen-containing compounds.
2. use:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride has a wide range of applications in organic synthesis. It is an important intermediate for the preparation of compounds with biological activity. For example, it can be used to synthesize drugs, pesticides and other biologically active molecules. In addition, it can also be used to synthesize functional polymers and coating materials.
3. Preparation method:
The preparation method of 4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is generally obtained by reacting 4-(1,2,3-thiadiazol-4-yl) benzoic acid with astatine chloride or arsenic chloride under appropriate conditions. The specific reaction conditions can be adjusted according to actual needs.
4. Safety Information:
4-(1,2,3-thiadiazol-4-yl)benzoyl chloride is an irritating compound and is corrosive. Wear appropriate protective equipment such as glasses, gloves, and lab coats when handling the compound. Avoid contact with skin and eyes. It should be operated in a well-ventilated place to avoid inhaling its vapors. If you come into contact with this compound, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 15:17:57
