CAS 391864-01-0

3-Chloro-N-(5-ethyl-1,3,4-thiadiazol-2-yl)propanamide

Description:

3-Chloro-N-(5-ethyl-1,3,4-thiadiazol-2-yl)propanamide is a chemical compound characterized by its unique structure, which includes a chloro group and a thiadiazole moiety. The presence of the chloro substituent suggests potential reactivity, particularly in nucleophilic substitution reactions. The thiadiazole ring contributes to the compound's biological activity, often associated with antimicrobial or herbicidal properties. The ethyl group enhances the lipophilicity of the molecule, potentially influencing its solubility and permeability in biological systems. As a propanamide derivative, it features an amide functional group, which can participate in hydrogen bonding, affecting its physical properties such as melting point and boiling point. This compound may be of interest in pharmaceutical research and agrochemical applications due to its structural characteristics and potential bioactivity. Safety and handling precautions should be observed, as with any chemical substance, particularly those containing halogens and nitrogen heterocycles.

Formula: C₇H₁₀ClN₃OS

InChI: InChI=1S/C7H10ClN3OS/c1-2-6-10-11-7(13-6)9-5(12)3-4-8/h2-4H2,1H3,(H,9,11,12)

InChI key: InChIKey=CBIHUHXXBJILSQ-UHFFFAOYSA-N

SMILES: N(C(CCCl)=O)C=1SC(CC)=NN1

Synonyms:

• propanamide, 3-chloro-N-(5-ethyl-1,3,4-thiadiazol-2-yl)-
• 3-Chloro-N-(5-ethyl-1,3,4-thiadiazol-2-yl)propanamide

3-chloro-N-(5-ethyl-1,3,4-thiadiazol-2-yl)propanamide

CAS: 391864-01-0

Formula: C₇H₁₀ClN₃OS

Purity: 95.0%

Molecular weight: 219.69

Ref: 10-F314873