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| 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI& Basic information |
Product Name: | 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI& | Synonyms: | 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI&;1,3,4-Thiadiazol-2-amine, 5-(4-fluorophenyl)-;5-(4-fluorophenyl)-1,3,4-thiadiazol-2-amine(SALTDATA: FREE);5-(4-Fluorophenyl)-1,3,4-thiadiazol-2-amine, 1-(5-Amino-1,3,4-thiadiazol-2-yl)-4-fluorobenzene;2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazole 97%;JRH-02707, 5-(4-Fluorophenyl)-1,3,4-thiadiazol-2-amine, 97% | CAS: | 942-70-1 | MF: | C8H6FN3S | MW: | 195.22 | EINECS: | | Product Categories: | API intermediates;Building Blocks;Chemical Synthesis;Fluorinated Building Blocks;Heterocyclic Building Blocks;Heterocyclic Fluorinated Building Blocks;Other Fluorinated Heterocycles;Thiadiazoles | Mol File: | 942-70-1.mol | |
| 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI& Chemical Properties |
Hazard Codes | Xn | Risk Statements | 22-36 | Safety Statements | 26 | WGK Germany | 3 | HS Code | 2934999090 |
| 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI& Usage And Synthesis |
Uses | 2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazole can be used as a substrate in the preparation of:
- Bithiophene based azo dyes with possible nonlinear optical (NLO) properties.
- 4-Thiazolidinone derivatives as potent HCV NS5B polymerase inhibitors.
- 1,3,4-Thiadiazole and phenothiazine hybrids as possible antitubercular agents.
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| 2-AMINO-5-(4-FLUOROPHENYL)-1 3 4-THIADI& Preparation Products And Raw materials |
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