thiazole


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Related to thiazole: thiazole orange

thi·a·zole

 (thī′ə-zōl′)
n.
1. A colorless or pale yellow aromatic liquid, C3H3NS, containing a ring composed of a nitrogen atom, a sulfur atom, and three carbon atoms, used in making dyes and fungicides.
2. Any of various derivatives of this compound.

thiazole

(ˈθaɪəˌzəʊl) or

thiazol

n
1. (Chemistry) a colourless liquid with a pungent smell that contains a ring system composed of three carbon atoms, a sulphur atom, and a nitrogen atom. It is used in dyes and fungicides. Formula: C3H3NS
2. (Elements & Compounds) any of a group of compounds derived from this substance that are used in dyes

thi•a•zole

(ˈθaɪ əˌzoʊl)

n.
1. a colorless, slightly water-miscible liquid, C3H3NS.
2. any of various derivatives of this substance, used as dyes or reagents.
[1885–90]
Translations
thiazole
References in periodicals archive ?
The reason behind the overall market growth could be its use as an intermediate for developing thiazole and other drugs for inhibiting thyroid disease.
Akroform MTT-80/EPR/P is a type of thiazole heterocyclic compound used for crosslinking halogen-containing polymers.
Saracoglu, Quantum chemical and molecular dynamics simulation studies on inhibition performances of some thiazole and thiadiazole derivatives against corrosion of iron, J.
Pocket modeling of the SEC revealed the binding pocket of SEC is U-shaped and highly hydrophobic, keeping in mind complementary structures on the thiazole template were designed with structural modification on the aromatic moiety carried out.
Mostly, they are thiazole derivatives critically involved in arresting viral replication in cell-based assays (54).
Imidazole, triazole, and thiazole derivatives exhibited the antifungal activity against a broad spectrum of fungi [29].
A subset of 34 Tox21 compounds was purchased from Sigma-Aldrich, except for 2-hydrazino-4-(4-aminophenyl) thiazole, which was obtained from Oakwood Chemical, and lasalocid sodium purchased from Santa Cruz Biotechnology.
FT-IR (KBr, [cm.sup.-1]): 3441 (O-H, s), 3045, 1460, and 753 (thiazole, m), 2964 and 2870 (C-H, m), 1601 and 1508 (Benz.
Underhill, "Cobalt(II), nickel(II), and copper(II) complexes of imidazole and thiazole," Journal of the Chemical Society A: Inorganic, Physical, Beoretical, pp.
Pelosi et al., "CPTH6, a thiazole derivative, induces histone hypoacetylation and apoptosis in human leukemia cells," Clinical Cancer Research, vol.