Hexythiazox-d11

CAS : 78587-05-0

Ref. TR-H298501

Informations sur le produit

• Nom: Hexythiazox-d11
• Synonymes: (4S,5S)-5-(4-chlorophenyl)-4-methyl-2-oxo-N-(1,2,2,3,3,4,4,5,5,6,6-undecadeuteriocyclohexyl)thiazolidine-3-carboxamide, (4R,5R)-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide, (4RS,5RS)-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide, (4S)-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide, (4S,5S)-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide, 3-Thiazolidinecarboxamide, 5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-, (4R,5R)-rel-, 3-Thiazolidinecarboxamide, 5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-, trans-, 5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide, Calibre, Cesar, Gwn 2106, Hexygon, Hexythiazox E.C., Maccomite, Maiden, Matacar, Na 73, Nissorun, Onager, Ordoval, Savey, Savey PM, Trans-5-(4-Chlorophenyl)-N-Cyclohexyl-4-Methyl-2-Oxo-3-Thiazolidinecarboxamide, Trevi, Zeldox, rel-(4R,5R)-5-(4-Chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-3-thiazolidinecarboxamide

Description

Applications A labelled form of Hexythiazox (H298500), which is a mite growth regulator and a thiazolidine based acaricide that has long-lasting effects against many kinds of mites and is applied at any stage of the plant growth from budding to fruiting. Useful in cannabis testing kits as a component of pesticide mixes (P698240).
References Martini,X., et al.: Pest. Manage. Sci., 68, 1471 (2012); Gilbert-Lopez, B., et al.: Food. Control., 26, 341 (2012);

• Marque: TRC

Propriétés chimiques

• Masse moléculaire: 363.95
• Formule: C₁₇D₁₁H₁₀ClN₂O₂S
• Couleur/Forme: White To Off-White
• InChI: InChI=1S/C17H21ClN2O2S/c1-11-15(12-7-9-13(18)10-8-12)23-17(22)20(11)16(21)19-14-5-3-2-4-6-14/h7-11,14-15H,2-6H2,1H3,(H,19,21)/t11-,15+/m0/s1/i2D2,3D2,4D2,5D2,6D2,14D
• Code InChI: InChIKey=XGWIJUOSCAQSSV-SLWLBTFMSA-N
• SMILES: [2H]C1([2H])C([2H])([2H])C([2H])([2H])C([2H])(NC(=O)N2C(=O)S[C@H](c3ccc(Cl)cc3)[C@@H]2C)C([2H])([2H])C1([2H])[2H]