Thiazines

Thiazines (also called 1,4-thiazines) consist of a six-membered ring containing a sulfur and a nitrogen atom para to each other. Thiazines exhibit diverse pharmacological and biological activities, such as anticancer, antimicrobial, anti-inflammatory, and antipyretic activities, as well as act as central nervous system depressants.

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CBR00886 1,3-Thiazinane-4-carboxylic acid hydrochloride AldrichCPR C5H10ClNO2S
640638 7-Bromo-2H-[1,4]-benzothiazin-3(4H)-one 97% C8H6BrNOS
543586 7-Chloro-2H-1,4-benzothiazin-3(4H)-one 97% C8H6ClNOS
175277 2H-1,4-Benzothiazin-3(4H)-one 97% C8H7NOS
CDS019817 6-Chloro-3,4-dihydro-2H-1,4-benzothiazine AldrichCPR C8H8ClNS
647519 7-Methyl-1,4-benzothiazin-3(4H)-one 97% C9H9NOS
647500 7-Methoxy-1,4-benzothiazin-3(4H)-one 97% C9H9NO2S
658332 6-Chloroacetyl-2H-1,4-benzothiazin-3(4H)-one 97% C10H8ClNO2S
630705 3,4-Dihydro-3-oxo-2H-(1,4)-benzothiazin-2-ylacetic acid C10H9NO3S
CDS012020 5-(4-Fluorophenyl)-3,4-dihydro-2H-1,4-thiazine-3-carboxylic acid AldrichCPR C11H10FNO2S
C63006 2-Chlorophenothiazine 97% C12H8ClNS
373559 2-Chlorophenothiazine 95% C12H8ClNS
88580 Phenothiazine purum, ≥98.0% (GC) C12H9NS
P14831 Phenothiazine ≥98% C12H9NS
CDS015049 1-[2-(4-chlorophenyl)-6h-1,3-thiazin-5-yl]ethan-1-one AldrichCPR C12H10ClNOS
552429 Ethyl 4-hydroxy-2-methyl-1,1-dioxo-2H-1,2-benzothiazine-3-carboxylate 97% C12H13NO5S
CDS019111 tert-Butyl (4aR,8aS)-octahydro-6H-pyrido[3,4-b][1,4]thiazine-6-carboxylate AldrichCPR C12H22N2O2S
175226 2-Acetylphenothiazine 95% C14H11NOS
8.16113 1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione 1,3,5-Triallyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione (stabilised) for synthesis. CAS 1025-15-6, molar mass 249.27 g/mol., (stabilised) for synthesis C₁₂H₁₅N₃O₃
1.11613 Ferrospectral Ferrospectral GR for analysis (reagent for iron). CAS 28048-33-1, molar mass 514.44 g/mol., GR for analysis (reagent for iron) C₂₀H₁₂N₄Na₂O₆S₂
1.10888 Dichloroisocyanuric acid sodium salt dihydrate Dichloroisocyanuric acid sodium salt dihydrate GR for analysis. CAS 51580-86-0, pH 6.7 (10 g/l, H₂O, 20 °C)., GR for analysis C₃Cl₂N₃NaO₃ * 2 H₂O
8.02815 Cyanuric chloride Cyanuric chloride for synthesis. CAS 108-77-0, pH (H₂O) acidic,Hydrolysis., for synthesis C₃Cl₃N₃
8.08607 Trichloroisocyanuric acid Trichloroisocyanuric acid for synthesis. CAS 87-90-1, pH 2.0 - 2.7 (10 g/l, H₂O, 20 °C)., for synthesis C₃Cl₃N₃O₃
8.41156 6-Azauracil 6-Azauracil for synthesis. CAS 461-89-2, molar mass 113.07 g/mol., for synthesis C₃H₃N₃O₂
8.20358 Cyanuric acid Cyanuric acid for synthesis. CAS 108-80-5, chemical formula C₃N₃(OH)₃., for synthesis C₃H₃N₃O₃
8.43815 1,3,5-Triazine-2,4,6(1H,3H,5H)-thrithione 1,3,5-Triazine-2,4,6(1H,3H,5H)-thrithione for synthesis. CAS 638-16-4, molar mass 177.27 g/mol., for synthesis C₃H₃N₃S₃
8.08614 2,4,6-Triamino-1,3,5-triazine 2,4,6-Triamino-1,3,5-triazine for synthesis. CAS 108-78-1, pH 7 - 8 (32 g/l, H₂O, 20 °C)., for synthesis C₃H₆N₆
8.18712 Hexamethylenetetramine Hexamethylenetetramine for synthesis. CAS 100-97-0, pH 7.0 - 9.0 (100 g/l, H₂O, 20 °C)., for synthesis C₆H₁₂N₄
8.03573 2,6-Diamino-4-phenyl-1,3,5-triazine 2,6-Diamino-4-phenyl-1,3,5-triazine for synthesis. CAS 91-76-9, pH 6.5 (0.3 g/l, H₂O, 20 °C)., for synthesis C₉H₉N₅