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acetamide's Usage Examples:

Piracetam is in the racetams group, with chemical name 2-oxo-1-pyrrolidine acetamide.

relationship of imines to amines having double and single bonds carries over to imides and amides, as in acetamide vs succinimide.

Neosalvarsan 1935 – Prontosil (an oral precursor to sulfanilamide), the first sulfonamide 1936 – Sulfanilamide 1938 – Sulfapyridine (M"B 693) 1939 – sulfacetamide.

"Topical sulfacetamide vs oral erythromycin for neonatal chlamydial conjunctivitis".

Bis(trimethylsilyl)acetamide (BSA) is an organosilicon compound with the formula Me3SiNC(OSiMe3)Me (Me CH3).

It is the main precursor to acetamide: NH4CH3CO2 → CH3C(O)NH2 + H2O It is also used as a diuretic.

"Effects of SUN-1165, N-(2,6-dimethylphenyl)-8-pyrrolizidine acetamide hydrochloride hemihydrate, a new class I antiarrhythmic drug, on ventricular.

Poly(N-vinylacetamide) (PNVA) is a polymer having affinity for both water and alcohol made primarily from N-vinylacetamide (NVA) monomer.

was first synthesised by the reaction of sodium cyanoacetamide with nitric acid.

The sulfacetamide inhibits the growth of the bacterium Cutibacterium acnes that is associated with acne, while sulfur facilitates the removal of dead.

(indol-3-yl)acetamide + CO2 + H2O Thus, the two substrates of this enzyme are L-tryptophan and O2, and its 3 products are (indol-3-yl)acetamide, CO2, and.

Sulfacetamide should not be used by individuals who have a sensitivity to sulfur or sulfa.

Common examples of amides are acetamide H3C–CONH2, benzamide C6H5–CONH2, and dimethylformamide HCON(–CH3)2.