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2,6-Dichloropyridine is a chloropyridine with the formula C 5 H 3 Cl 2 N. A white solid, it is one of six isomers of dichloropyridine . It serves as a precursor to the antibiotic enoxacin , [ 2 ] as well as the drug and anpirtoline and the antifungal liranaftate .
Sudocrem (/ ˈ s u d ə k r ɛ m / or / ˈ s u d ə k r i m / in Ireland) [3] is an over-the-counter medicated cream aimed primarily at the treatment of irritant diaper dermatitis.It contains a water-repellent base (consisting of oils/waxes); protective and moisturizer agents; antibiotic and antifungal agents; and a weak anesthetic.
Imiquimod is a patient-applied cream prescribed to treat genital warts, Bowens disease (squamous cell carcinoma in situ), and, secondary to surgery, for basal cell carcinoma, [7] [8] as well as actinic keratosis. [9] Imiquimod 5% cream is indicated for the topical treatment of: external genital and perianal warts (condylomata acuminata) in ...
Clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) is a selective herbicide used for control of broadleaf weeds, especially thistles and clovers.Clopyralid is in the picolinic acid family of herbicides, which also includes aminopyralid, picloram, triclopyr, and several less common herbicides.
Some dichlorotoluenes are precursors to commercial pesticides. 2,4-Dichlorotoluene is the precursor to pyrifenox, butafenacil, and the pyrazole derivatives pyrazoxyfen and [pyrazolynate]]. The 2,6 isomer is a precursor to dichlobenil (2,6-dichlorobenzonitrile). 3,5-Dichlorotoluene is used to prepare propyzamide. [2]
2,6-Dichloroquinone-4-chloroimide (Gibbs reagent) is an organic compound used as an colorimetric indicator to detect phenolic compounds. [1] Upon reaction with phenol itself, 2,6-dichlorophenolindophenol is formed, [ 2 ] a chemical that is used as a redox indicator .
In these conversions, chloride is displaced. [2] Pyrithione, the conjugate base of 2-mercaptopyridine-N-oxide, is a fungicide found in some shampoos. Oxidation 2-chloropyridine gives 2-chloropyridine-N-oxide. [5] The antihistamine pheniramine may be generated via the reaction of phenylacetonitrile with 2-chloropyridine in the presence of a base ...
It is primarily used for the treatment of herpes simplex virus infections, chickenpox, and shingles. [6] Other uses include, prevention of cytomegalovirus infections following transplant, and severe complications of Epstein–Barr virus infection. [6] [7] It can be taken by mouth, applied as a cream, or injected. [6]