Thiophanate-methyl-d6

CAS: 1398065-77-4

Ref. TR-T344812

Informação sobre produto

• Nome: Thiophanate-methyl-d6
• Sinónimos: N,N'-[1,2-Phenylenebis(iminocarbonothioyl)]biscarbamic-d6 Acid C,C'-Dimethyl Ester, 4,4'-o-Phenylenebis[3-thioallophanic-d6 Acid Dimethyl Ester, 1,2-Bis[3-(methoxycarbonyl)-2-thioureido]benzene-d6, 3336G-d6, Caligran-d6, Cercobin M 70-d6, Cercobin Methyl-d6, Cycosin-d6, Dimethyl 4,4'-o-Phenylenebis(3-thioallophanate)-d6, Easout-d6, Enovit M 70-d6, Enovit Super-d6, Enovit-methyl-d6, F 6385-d6, Fungo-d6, Methyl topsin-d6, Methylthiofanate-d6, Methylthiophanate-d6, Metoben-d6, Mildothane-d6, NF 44-d6, NSC 170811-d6, Neotopsin-d6, Thiopan-d6, Tops-d6, Topsin 500SC-d6, Topsin M 70WP-d6, Topsin MD-d6, Topsin Methyl-d6, o-Bis(3-methoxycarbonyl-2-thioureido)benzene-d6

Descrição

Applications Isotope labelled Thiophanate-methy (T344810)l, which is a systematic fungicide of the thiophanate class. Thiophanate-Methyl is commonly used in agriculture to protect against powdery mildew, rot and other fungal (1,2) diseases in fruits, vegetables and other crops (3). May also function as a pesticide with cocarcinogenesis effects on insects observed. Antihelmintic (4).Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References 1. Mahmoudi N. et al.: Antimicrob Agents Chemother. 2008 Apr;52(4):1215-20 2. Burchill, R. et al.: Plant Pathol. 1971 Dec:20(4);173-1763. Fuchs, A. et al.: Pest Biochem. Physiol. 1972:2(2);191-2054. Paolini, M. et al.: Cancer Lett. 1999 Jan 29;135(2):203-13.

• Marca: TRC

Propriedades químicas

• Peso molecular: 348.43
• Fórmula: C₁₂H₈D₆N₄O₄S₂
• Cor/forma: Neat
• InChI: InChI=1S/C12H14N4O4S2/c1-19-11(17)15-9(21)13-7-5-3-4-6-8(7)14-10(22)16-12(18)20-2/h3-6H,1-2H3,(H2,13,15,17,21)(H2,14,16,18,22)/i1D3,2D3
• Chave InChI: InChIKey=QGHREAKMXXNCOA-WFGJKAKNSA-N
• SMILES: [2H]C([2H])([2H])OC(=O)NC(=S)Nc1ccccc1NC(=S)NC(=O)OC([2H])([2H])[2H]