CAS 21521-87-9
:2-chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
Description:
2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide is a chemical compound characterized by its unique structure, which includes a chloro group and a thiadiazole moiety. The presence of the 5-methyl group on the thiadiazole ring contributes to its biological activity and solubility properties. This compound typically exhibits moderate to high stability under standard conditions, although it may be sensitive to strong acids or bases. It is often utilized in various fields, including pharmaceuticals and agrochemicals, due to its potential as a bioactive agent. The compound's molecular interactions can be influenced by the chloro substituent, which may enhance its reactivity and binding affinity in biological systems. Additionally, its acetamide functional group can participate in hydrogen bonding, affecting its solubility in polar solvents. Overall, 2-chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide is a versatile compound with significant implications in chemical research and application.
Formula:C5H6ClN3OS
InChI:InChI=1/C5H6ClN3OS/c1-3-8-9-5(11-3)7-4(10)2-6/h2H2,1H3,(H,7,9,10)
InChI key:YDRMIMUGNZLYMQ-UHFFFAOYSA-N
SMILES:Cc1nnc(N=C(CCl)O)s1
Synonyms:- Acetamide, 2-chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)-
- 2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
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2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
CAS:2-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamideFormula:C5H6ClN3OSPurity:97%Molecular weight:191.638642-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
CAS:Formula:C5H6ClN3OSPurity:97%Color and Shape:SolidMolecular weight:191.63862-Chloro-N-(5-methyl-1,3,4-thiadiazol-2-yl)acetamide
CAS:Formula:C5H6ClN3OSPurity:97%Molecular weight:191.63



