663557
2-Amino-5-(4-fluorophenyl)-1,3,4-thiadiazole
97%
Synonym(s):
5-(4-Fluorophenyl)-1,3,4-thiadiazol-2-amine
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About This Item
Empirical Formula (Hill Notation):
C8H6FN3S
CAS Number:
Molecular Weight:
195.22
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
238-243 °C
SMILES string
Nc1nnc(s1)-c2ccc(F)cc2
InChI
1S/C8H6FN3S/c9-6-3-1-5(2-4-6)7-11-12-8(10)13-7/h1-4H,(H2,10,12)
InChI key
WRSVCKNLHZWSNJ-UHFFFAOYSA-N
Application
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.[1]
- 4-Thiazolidinone derivatives as potent HCV NS5B polymerase inhibitors.[2]
- 1,3,4-Thiadiazole and phenothiazine hybrids as possible antitubercular agents.[3]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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2-Heteroarylimino-5-arylidene-4-thiazolidinones as a new class of non-nucleoside inhibitors of HCV NS5B polymerase
Kucukguzel ?, et al.
European Journal of Medicinal Chemistry, 69(2), 931-941 (2013)
Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
Castro MR, et al.
Dyes and Pigments, 95(2), 392-399 (2012)
Design of new phenothiazine-thiadiazole hybrids via molecular hybridization approach for the development of potent antitubercular agents
Ramprasad J, et al.
European Journal of Medicinal Chemistry, 106(2), 75-84 (2015)
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