有机硫化合物是指含有硫原子的有机化合物。这些化合物在自然界中广泛存在,在医药、农药和材料科学等领域有着重要的应用。有机硫化合物因其化学性质独特,在药物设计、合成化学以及材料制备方面扮演着重要角色。
1. 结构与分类有机硫化合物可以按硫的连接方式分为饱和和不饱和类,如二硫化物、噻吩衍生物、砜等。常见的结构类型有:
许多有机硫化合物在生物学上有重要功能或应用潜力。例如:
有机硫化合物可通过多种途径合成:
有机硫化合物的应用广泛:
尽管有机硫化合物具有许多潜在益处,但其生产和使用也可能对环境造成影响。因此,在设计和合成这些化合物时需要考虑可持续性和环保性因素。
以上是对有机硫化合物的简单介绍,包括它们的结构、生物学活性、合成方法及其应用领域等基本信息。
中文名称 | 英文名称 | CAS号 | 化学式 | 结构式图片 |
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—— | 3-bromo-4-<(bromomethyl)sulfonyl>-hex-3-ene | —— | C7H12Br2O2S |
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—— | 5-amino-2,3-dihydro-N,N-dipropyl-3-benzothiophenecarboxamide | —— | C15H22N2OS |
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—— | 2-(4'-methylthiophenoxy)tetrahydrothiophene | —— | C11H14S2 |
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—— | 5-((4-chlorophenyl)thio)pentanenitrile | —— | C11H12ClNS |
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—— | 5-((3-chlorophenyl)thio)pentanenitrile | —— | C11H12ClNS |
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—— | 5-((3,4-difluorophenyl)thio)pentanenitrile | —— | C11H11F2NS |
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—— | 5-((3,4-dimethylphenyl)thio)pentanenitrile | —— | C13H17NS |
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—— | (3-bromopropyl)(dodecyl)sulfane | —— | C15H31BrS |
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—— | tert-butyl(dodecyl)sulfane | —— | C16H34S |
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—— | (Z)-3-dodecylthio-2-propen-1-ol | —— | C15H30OS |
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—— | 3,4-bis(dodecylthio)thiophene | —— | C28H52S3 |
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—— | (2-dodecylsulfide)selenophene | —— | C16H28SSe |
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—— | 1-Dodecanethiolchloride | —— | C12H25ClS |
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—— | 2-(dodecylthio)-1,3-benzoselenazole | —— | C19H29NSSe |
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—— | 2,6-di-tert-butyl-4-pyridyl dodecyl sulfide | —— | C25H45NS |
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—— | 4-((4,6-dimethoxypyrimidin-2-yl)thio)-2-(trifluoromethyl)benzoic acid | —— | C14H11F3N2O4S |
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—— | trithiocarbonic acid dodecyl ester propyl ester | —— | C16H32S3 |
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—— | 3-chloro-5-methylphenyl dodecyl sulfide | —— | C19H31ClS |
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—— | dodecanethiol-D1 | —— | C12H26S |
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—— | 2-(2,3-dihydrobenzo[b]thiophen-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | —— | C14H19BO2S |
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—— | (2S,2'S)-2,3,2',3'-tetrahydro-2,2'-bi(benzo[b]thiophenyl) | —— | C16H14S2 |
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—— | meso-2,3,2',3'-tetrahydro-2,2'-bi(benzo[b]thiophenyl) | —— | C16H14S2 |
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—— | (2R,2'R)-2,3,2',3'-tetrahydro-2,2'-bi(benzo[b]thiophenyl) | —— | C16H14S2 |
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—— | 2-Azido-2,3-dihydrobenzothiophene | —— | C8H7N3S |
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—— | 2-(4-bromophenylthio)-1-(4-chlorophenyl)ethanol | —— | C14H12BrClOS |
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—— | 2-((1-(4-chlorophenyl)ethyl)thio)pyridine | —— | C13H12ClNS |
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—— | 2,3,5-trichloro-4,6-bis(isopropylsulfanyl)pyridine | —— | C11H14Cl3NS2 |
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—— | Isopentyl-<2-methyl-cyclohexyl>-sulfid | —— | C12H24S |
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—— | ethyl 5-(isopentylthio)-2-methyl-1H-pyrrole-3-carboxylate | —— | C13H21NO2S |
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—— | 3-(isopropylthio)pyridine | —— | C8H11NS |
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—— | Thiosemiquadratsaeure-S-isopropylester | —— | C7H8O2S |
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—— | 3,5-dichloro-2,4,6-tris(isopropylsulfanyl)pyridine | —— | C14H21Cl2NS3 |
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—— | 3-[(1-methylethyl)sulfanyl]propan-1-ol | —— | C6H14OS |
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—— | thioisovaleraldehyde | —— | C5H10S |
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—— | 3-fluoro-2-isopropylthiopyridine | —— | C8H10FNS |
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—— | 2-(4-bromophenylthio)-1-(4-fluorophenyl)ethanol | —— | C14H12BrFOS |
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—— | 6,6-Dimethyl-3-isopropylthio-1-(pyrazol-3-yl)-4,5,6,7-tetrahydrobenzo[c]thiophen-4-one | —— | C16H20N2OS2 |
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—— | 3-bromo-6-(isopropylthio)-2-methylpyridine | —— | C9H12BrNS |
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—— | 2-(isopropyldisulfaneyl)ethan-1-ol | —— | C5H12OS2 |
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—— | 5-((1-(4-fluorophenyl)ethyl)thio)-1-methyl-1H-tetrazole | —— | C10H11FN4S |
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—— | 2,4-bis(isopropylthio)-6-methyl-3-nitropyridine | —— | C12H18N2O2S2 |
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—— | 3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)-methyl-7-(ethoxycarbonyl)-6-methyl-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine | —— | C14H16N6O4S |
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—— | 3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)-methyl-6-phenyl-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine | —— | C16H14N6O2S |
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—— | 3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)-methyl-6-(ethoxycarbonylmethyl)-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazine | —— | C14H16N6O4S |
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—— | 3-(6-methyl-2,4-dioxo-1,2,3,4-tetrahydro-3-pyrimidinyl)-methyl-7H-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazin-6-ylamine | —— | C10H11N7O2S |
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—— | 6-Cyclohexylthio-1-ethoxymethyl-5-isopropyluracil | —— | C16H26N2O3S |
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—— | cyclohex-1-en-1-yl(cyclohexyl)sulfane | —— | C12H20S |
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—— | S-cyclohexyl-N,N-diethylcarbamate | —— | C11H21NOS |
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—— | Dicyclohexylsulfidmethiodid | —— | C13H25S*I |
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—— | β-<4-Fluor-phenylmercapto>-isopropanol | —— | C9H11FOS |
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