thiosemicarbazide


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thiosemicarbazide

[¦thī·ō‚sem·i′kär·bə‚zīd]
(organic chemistry)
NH2CSNHNH2 A white, water- and alcohol-soluble powder melting at 182°C; used as an analytical reagent and in photography and rodenticides.
References in periodicals archive ?
[30] Raman N, Selvan A, Manisankar P Spectral, magnetic, biocidal screening, DNA binding and photocleavage studies of mononuclear Cu(II) and Zn(II) metal complexes of tricoordinate heterocyclic Schiff base ligands of pyrazolone and semicarbazide/ thiosemicarbazide based derivatives, Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 76: 161-173, 2010.
El-Asmy, "Physical and spectroscopic studies on novel vanadyl complexes of some substituted thiosemicarbazides," Spectrochimica Acta Part A, vol.
This electronic density can be attributed to autocondensation of thiosemicarbazide, generating [H.sub.2]S as a subproduct.
Representative Procedure for the Synthesis of 1-(4Fluorophenyl)-1,3-dihydroisobenzofuran-5-acyl Thiosemicarbazides 11(a-h).
The reaction product (III) and thiosemicarbazide were refluxed for 3 h in dilute hydrochloric acid.
Campbell, "Transition metal complexes of thiosemicarbazide and thiosemicarbazones," Coordination Chemistry Reviews, vol.
Synthesis of two series, 20,21(a-c), of Mannich bases of 1,5-benzodiazepines was carried out and evaluated for the anticonvulsant activity by isoniazid and thiosemicarbazide induced convulsion model (Figures 20 and 21).
Ethanol solution (15 ml) of VBOPE (1 mmol) was added dropwise to a solution of thiosemicarbazide hydrochloride (1.1 mmol) and pyridine (1.1 mmol) in ethanol at room temperature, and the mixture was refluxed for 12 h at 70[degrees]C and then cooled and poured slowly into excess water (32).
Benzoic acid (0.1 mol) and thiosemicarbazide (0.1 mol) in phosphorous oxychloride (30 mL) were refluxed gently for 30 min and cooled followed by careful addition of water (90 mL).
Firstly, Hthiomen was prepared from thiosemicarbazide and ([+ or -]) menthone (1: 1 molar ratio).
A mixture of thiosemicarbazide (1.0 M), Carbon disulphide (1.2 M) and dimethyl formamide (40 mL) was refluxed for 3 h.