| Weight | 120.564 g/mol |
|---|---|
| Formula | C2HClN2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
5-Chloro-1,2,4-thiadiazole (38362-15-1)
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- Intermolecular Magnetic Couplings in the Dinuclear Copper(II) Complex -Chloro--[2,5-bis(2-pyridyl)-1,3,4-thiadiazole] Aqua Chlorocopper(II) Dichlorocopper(II): Synthesis, Crystal Structure, and EPR and Magnetic Characterization (Inorganic Chemistry, 2004)
- Carbonic anhydrase inhibitors: X-ray crystallographic studies for the binding of 5-amino-1,3,4-thiadiazole-2-sulfonamide and 5-(4-amino-3-chloro-5-fluorophenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide to human isoform II. (Bioorganic & Medicinal Chemistry Letters, 2006)
- Ring transformations of 5-chloro-1,2,3-thiadiazole-4-carbaldehyde with amines, hydrazines and hydroxylamine (Journal of The Chemical Society-perkin Transactions 1, 1991)
- SYNTHESIS AND ANTICONVULSANT ACTIVITY OF NOVEL 2-AMINO-5-[4-CHLORO-2-(2-CHLOROPHENOXY) PHENYL]-1,3,4-THIADIAZOLE DERIVATIVES (DARU, 2007)
- Synthesis and Reactivity of 4(2Chloro5nitrophenyl)1,2,3thiadiazole. A Novel OnePot Synthesis of NSubstituted Indole2thiols. (Journal of Organic Chemistry, 2007)
- 3D- QSAR STUDIES, BIOLOGICAL EVALUATION STUDIES ON SOME SUBSTITUTED 3-CHLORO-1-(5-(5-CHLORO-2-PHENYL-BENZIMIDAZOLE-1- YLMETHYL)-(1, 3, 4) THIADIAZOLE-2-YL)-AZETIDIN-2-ONE AS POTENTIAL ANTIMICROBIAL ACTIVITY (2009)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESC1=NSC(=N1)Cl
-
InChIKeyRZKVGQCJNANFDR-UHFFFAOYSA-N
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