pyridine sulfonamide - meaning and definition. What is pyridine sulfonamide
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What (who) is pyridine sulfonamide - definition

CHEMICAL COMPOUND
Pyridine-sulfur trioxide; C5H5NSO3

sulphonamide         
CLASS OF CHEMICAL COMPOUNDS
Sulphonamides; Sulphonamide; Sulphonamide (chemistry); Sulfonamide (chemistry); Sulfonamides; Sultam
[s?l'f?n?m??d]
(US sulfonamide)
¦ noun Medicine any of a class of drugs, derived from sulphanilamide, which are able to prevent the multiplication of some pathogenic bacteria.
Origin
C19: from sulphone + amide.
Sulfonamide         
CLASS OF CHEMICAL COMPOUNDS
Sulphonamides; Sulphonamide; Sulphonamide (chemistry); Sulfonamide (chemistry); Sulfonamides; Sultam
In chemistry, the sulfonamide functional group (also spelled sulphonamide) is -S(=O)2-NH2, a sulfonyl group connected to an amine group. Relatively speaking this group is unreactive.
sulpha         
  • [[Furosemide]] is a sulfonamide, but not a thiazide.
  • [[Hydrochlorothiazide]] is a sulfonamide and a [[thiazide]].
  • PABA]] (center) is the basis for the inhibitory activity of sulfa drugs on tetrahydrofolate (right) biosynthesis.
  • [[Sulfamethoxazole]] is an antibacterial sulfonamide
CLASS OF PHARMACEUTICAL DRUGS
Sulfa Drugs; Sulfa drugs; Sulfa; Sulpha; Sulfa drug; Sulfa powder; Sulphonamide (medicine); Sulpha drugs; Sulpha drug; Sulfa antibiotic; Sulfonamide antibiotics; Sulfonamide allergy; Sulfa allergy
['s?lf?]
(US sulfa)
¦ noun [usu. as modifier] short for sulphonamide: sulpha drugs.

Wikipedia

Sulfur trioxide pyridine complex

Sulfur trioxide pyridine complex is the compound with the formula C5H5NSO3. It is a colourless solid that dissolves in polar organic solvents. It is the adduct formed from the Lewis base pyridine and the Lewis acid sulfur trioxide. The compound is mainly used as a source of sulfur trioxide, for example in the synthesis of sulfate esters from alcohols:

ROH + C5H5NSO3 → [C5H5NH]+[ROSO3]

It also is useful for sulfamations:

R2NH + C5H5NSO3 → C5H5N + R2NSO3H

The compound is used for sulfonylation reactions, especially in the sulfonylation of furans. It is also an activating electrophile in a Parikh-Doering oxidation.