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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—— | 2,11-dithiadodeca-3,5,7,9-tetrayne | —— | C10H6S2 |
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—— | S-methyl N-(1,1-dimethyl-3-oxobutyl)thiocarbamate | —— | C8H15NO2S |
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—— | 3-(methanesulfanyl)-2-propyn-1-ol | —— | C4H6OS |
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—— | 2-chloro-6-propylsulfanylpyridine | —— | C8H10ClNS |
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—— | 2-(methylthio)-1-azetine | —— | C4H7NS |
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—— | 8-((3,5-dichlorophenyl)thio)-9H-purin-6-amine | —— | C11H7Cl2N5S |
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—— | (1-Methylthiopropyliden)cyclohexan | —— | C10H18S |
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—— | (S)-1-Methylsulfonylheptan-2-ol | —— | C8H18O3S |
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—— | 1-Methylsulfonylheptan-2-ol | —— | C8H18O3S |
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—— | S-2-(1-methyl)imidazolyl ethanethioate | —— | C6H8N2OS |
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—— | 5-butyl-4-ethoxy-2,6-bis(methylthio)pyrimidine | —— | C12H20N2OS2 |
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—— | O-tert-butyl azetidine-1-carbothioate | —— | C8H15NOS |
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—— | 4-bromobutanethiol | —— | C4H9BrS |
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—— | 1-methyl-2-((2-nitrophenyl)thio)-1H-imidazole | 133303-52-3 | C10H9N3O2S |
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—— | (E)-5-[(1,1-dimethylethyl)thio]-4-penten-2-ynenitrile | —— | C9H11NS |
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—— | 1-methyl-2-(p-tolylsulfanyl)-1H-imidazole | —— | C11H12N2S |
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—— | 2-ethylhexyl 3-((2-(azetidin-1-yl)-3-chloropyridin-4-yl)thio)propionate | —— | C19H29ClN2O2S |
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—— | 2-((2,4-dimethoxyphenyl)thio)benz[d]oxazole | —— | C15H13NO3S |
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—— | (4-chlorophenyl)(2,4-dimethoxyphenyl)sulfane | —— | C14H13ClO2S |
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—— | 1-(((ethylthio)carbonyl)oxy)-2-methylpropyl pivalate | —— | C12H22O4S |
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—— | 2-butylsulfanyl-5-phenyl[1,3,4]oxadiazole | —— | C12H14N2OS |
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—— | 3-(1-chloro-ethylsulfanyl)-propene | —— | C5H9ClS |
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—— | 5-(2-chlorophenyl)-2-(butylthio)-1,3,4-oxadiazole | —— | C12H13ClN2OS |
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—— | (R)-n-dodecyl 2-propyl sulfoxide | —— | C15H32OS |
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—— | (S)-tert-butyl isopropyl sulfoxide | —— | C7H16OS |
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—— | methyl(4-(prop-1-yn-1-yl)phenyl)sulfane | —— | C10H10S |
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—— | 1-benzyl-3-ethyl-2-phenylsulfanyl-1H-imidazolium bromide | —— | Br*C18H19N2S |
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—— | 2-(dimethyl(oxo)-λ<sup>6</sup>-sulfaneylidene)acetaldehyde | —— | C4H8O2S |
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—— | trans-4-Phenylthio-2,2-dimethyl-5-phenyl-4,5-dihydrofuran-3(2H)-one | —— | C18H18O2S |
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—— | 5-isopropyl-2-methylthio-1,3,4-thiadiazole | —— | C6H10N2S2 |
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—— | 4-methyl-4-(p-tolylsulfanylmethyl)hept-6-en-2-one | —— | C16H22OS |
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—— | 3,3-dimethyl-1-butenesulfinylmethyl methyl ketone | —— | C9H16O2S |
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—— | O-(1-isobutanoyloxyethyl) S-phenyl thiocarbonate | —— | C13H16O4S |
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—— | (4S)-4-tert-butyl-4,5-dihydro-2-<2-(phenylsulfanyl)phenyl>-1,3-oxazole | —— | C19H21NOS |
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—— | 4'-methylthio-1-trimethylsilyloxytoluene | —— | C11H18OSSi |
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—— | 2-(2-cyanophenylthio)pyrimidine | —— | C11H7N3S |
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—— | 2-[(4-nitrophenyl)thio]benzonitrile | —— | C13H8N2O2S |
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—— | 2-(2-bromophenylsulfanyl)benzonitrile | —— | C13H8BrNS |
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—— | 2-((3-methoxyphenyl)thio)benzonitrile | —— | C14H11NOS |
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—— | 2-((2-chlorophenyl)thio)benzonitrile | —— | C13H8ClNS |
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—— | N-methyl-(1-methyl-2-phenylvinyl)-2,2-bis(phenylsulfanyl)acetamide | —— | C24H23NOS2 |
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—— | 6-hydroxy-6-methyl-5-phenylthio-hepta-1,4(Z)-diene | —— | C14H18OS |
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—— | 2-fluoro-6-((1,1,1-trifluoro-2-methyl-3-(phenylthio)but-3-en-2-yl)oxy)pyridine | 1498084-49-3 | C16H13F4NOS |
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—— | 2-(benzylthio)-6-fluoropyridine | —— | C12H10FNS |
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—— | 4-ethylthio-2,6-pyridine dihydrazide | —— | C7H13N5S |
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—— | N-(4-methylthio-phenyl)-4-fluorobenzamidine | —— | C14H13FN2S |
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—— | 4-((3-methoxyphenyl)thio)benzonitrile | —— | C14H11NOS |
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—— | phenyl sulphide aldehyde | —— | C7H6OS |
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—— | (4-fluorophenylthio)acetylhydrazine | —— | C8H9FN2OS |
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—— | 3-(benzo[d]thiazol-2-ylthio)benzonitrile | —— | C14H8N2S2 |
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