| Weight | 241.113 g/mol |
|---|---|
| Formula | C8H5BrN2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
4-(4-Bromophenyl)-1,2,3-thiadiazole (40753-13-7)
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- Discovery of 2-(4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-bromophenyl)-1-(2-chlorophenyl)-1H-pyrazol-3-yl)-5-tert-butyl-1,3,4-thiadiazole (GCC2680) as a potent, selective and orally efficacious cannabinoid-1 receptor antagonist (Bioorganic & Medicinal Chemistry, 2010)
- Efficient Synthesis of Conjugated 1,3,4-Thiadiazole Hybrids through Palladium-Catalyzed Cross-Coupling of 2,5-Bis(4-bromophenyl)-1,3,4-thiadiazole with Boronic Acids (Synlett, 2015)
- 3-(4-bromophenyl)-5-methylsulfonyl-1,2,4- thiadiazole, procedure for its preparation, its use as a fungicide and novel intermediates (1992)
- Synthesis, spectroscopy and crystal structure of 2-cyclohexyl-5-formyl-6-(4-bromophenyl)imidazo[2,1-b][1,3,4]thiadiazole (Journal of Chemical Research-s, 2008)
- Suzuki coupling of functionalized arylboronic acids to a 2-Amino-5-(4-bromophenyl)-1,3,4-thiadiazole scaffold (2014)
- Copper(I) iodide-catalyzed synthesis of 1-benzothiophen-2-amines from 4-(2-bromophenyl)-1,2,3-thiadiazole (Russian Journal of Organic Chemistry, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC=C1C2=CSN=N2)Br
-
InChIKeyHGWOTVRPRHVJQK-UHFFFAOYSA-N
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