Atomfair 1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)- C3H2F3N3S

Description 1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)- (CAS No. 10444-89-0) is a high-purity heterocyclic organic compound with the molecular formula C3H2F3N3S . This specialized chemical features a thiadiazole core substituted with a trifluoromethyl group and an amine functionality, making it a valuable intermediate for pharmaceutical and agrochemical research. Its unique structure offers excellent reactivity for derivatization and functionalization in synthetic chemistry applications. Available in various quantities, this compound is rigorously tested for quality, ensuring consistency for demanding laboratory and industrial applications. Store in a cool, dry place away from light and moisture to maintain stability.

Description

1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)- (CAS No. 10444-89-0) is a high-purity heterocyclic organic compound with the molecular formula C₃H₂F₃N₃S. This specialized chemical features a thiadiazole core substituted with a trifluoromethyl group and an amine functionality, making it a valuable intermediate for pharmaceutical and agrochemical research. Its unique structure offers excellent reactivity for derivatization and functionalization in synthetic chemistry applications. Available in various quantities, this compound is rigorously tested for quality, ensuring consistency for demanding laboratory and industrial applications. Store in a cool, dry place away from light and moisture to maintain stability.

CAS No: 10444-89-0
Molecular Formula: C3H2F3N3S
Molecular Weight: 169.13
Exact Mass: 168.99215274
Monoisotopic Mass: 168.99215274
IUPAC Name: 5-(trifluoromethyl)-1,3,4-thiadiazol-2-amine
SMILES: C1(=NN=C(S1)N)C(F)(F)F
Synonyms: 10444-89-0, 2-Amino-5-trifluoromethyl-1,3,4-thiadiazole, 5-(Trifluoromethyl)-1,3,4-thiadiazol-2-amine, 2-Amino-5-(trifluoromethyl)-1,3,4-thiadiazole, 1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-

Application

1,3,4-Thiadiazol-2-amine, 5-(trifluoromethyl)-, is widely utilized as a key building block in medicinal chemistry for the synthesis of bioactive molecules, including potential antiviral and antibacterial agents. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in drug discovery. Researchers also employ this compound in agrochemical development for designing novel pesticides and herbicides. Additionally, it serves as a precursor for advanced materials and coordination chemistry studies.

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