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-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-(1-cyanocyclopentyl)acetamide | —— | C16H15ClN4O2S |
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—— | (2S)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-pyrrolidin-1-ylpropan-1-one | —— | C15H16ClN3O2S |
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—— | (2S)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-cyclohexylpropanamide | —— | C17H20ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-(1-cyanocyclohexyl)-N-methylacetamide | —— | C18H19ClN4O2S |
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—— | (2R)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-cyclopentylpropanamide | —— | C16H18ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[1-[(2S)-1-methoxypropan-2-yl]-2,5-dimethylpyrrol-3-yl]ethanone | —— | C20H22ClN3O3S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1R)-1-thiophen-2-ylethyl]acetamide | —— | C16H14ClN3O2S2 |
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—— | 2-(4-bromo-2-methylphenyl)sulfanyl-N-methylacetamide | —— | C10H12BrNOS |
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—— | N-(1-adamantylmethyl)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetamide | —— | C21H24ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-pentan-3-ylacetamide | —— | C15H18ClN3O2S |
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—— | (2S)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1R)-1-(4-fluorophenyl)ethyl]propanamide | —— | C19H17ClFN3O2S |
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—— | 1-(4-acetyl-3,5-dimethyl-1H-pyrrol-2-yl)-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]ethanone | —— | C18H16ClN3O3S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1S,2R)-2-methylcyclohexyl]acetamide | —— | C17H20ClN3O2S |
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—— | 2-[[5-(3-Chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetonitrile | —— | C10H6ClN3OS |
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—— | (2R)-N-benzyl-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanamide | —— | C18H16ClN3O2S |
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—— | N-benzyl-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-ethylacetamide | —— | C19H18ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[(2R,6R)-2,6-dimethylmorpholin-4-yl]ethanone | —— | C16H18ClN3O3S |
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—— | 2-[[5-(3-Chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[1-(2-methoxyethyl)-2,5-dimethylpyrrol-3-yl]ethanone | —— | C19H20ClN3O3S |
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—— | N-[(2R)-butan-2-yl]-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetamide | —— | C14H16ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(3R)-1,1-dioxothiolan-3-yl]acetamide | —— | C14H14ClN3O4S2 |
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—— | N-benzyl-N-tert-butyl-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetamide | —— | C21H22ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1R)-1-phenylethyl]acetamide | —— | C18H16ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-cyclopropylacetamide | —— | C13H12ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1R,2R)-2-methylcyclohexyl]acetamide | —— | C17H20ClN3O2S |
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—— | 2-(3-Chlorophenyl)-5-[(5-phenyl-1,3,4-oxadiazol-2-yl)methylsulfanyl]-1,3,4-oxadiazole | —— | C17H11ClN4O2S |
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—— | N-[(2S)-butan-2-yl]-2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]acetamide | —— | C14H16ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-propan-2-ylacetamide | —— | C13H14ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-(2-phenylethyl)acetamide | —— | C18H16ClN3O2S |
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—— | 2-(3-Chlorophenyl)-5-[(4-methylphenyl)methylsulfanyl]-1,3,4-oxadiazole | —— | C16H13ClN2OS |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-1-[(2S,6R)-2,6-dimethylmorpholin-4-yl]ethanone | —— | C16H18ClN3O3S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(2R)-4-phenylbutan-2-yl]acetamide | —— | C20H20ClN3O2S |
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—— | 2-[[5-(3-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(1S,2S)-2-methylcyclohexyl]acetamide | —— | C17H20ClN3O2S |
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—— | [2-Oxo-2-(2-phenylsulfanylanilino)ethyl] 3-ethyl-5-methyl-1,2-oxazole-4-carboxylate | —— | C21H20N2O4S |
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—— | 2-propan-2-ylsulfanyl-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C9H16N3OS+ |
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—— | [(1S)-1-[5-[(3-chlorophenyl)methylsulfanyl]-1,3,4-oxadiazol-2-yl]-2-methylpropyl]azanium | —— | C13H17ClN3OS+ |
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—— | (3R)-3-(4-chloro-3-methylphenyl)sulfanylpyrrolidine | —— | C11H14ClNS |
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—— | (3S)-3-(4-chloro-3-methylphenyl)sulfanylpyrrolidine | —— | C11H14ClNS |
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—— | (2S)-2-[(4-fluoro-3-methylphenyl)sulfanylmethyl]pyrrolidine | —— | C12H16FNS |
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—— | 2-[2-(1,3-Dioxan-2-yl)ethylsulfanyl]-5-pyridin-4-yl-1,3,4-oxadiazole | —— | C13H15N3O3S |
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—— | (2R)-2-[(4-fluoro-2-methylphenyl)sulfanylmethyl]pyrrolidine | —— | C12H16FNS |
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—— | (2R)-2-[(4-fluoro-3-methylphenyl)sulfanylmethyl]pyrrolidine | —— | C12H16FNS |
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—— | (2S)-2-[(4-fluoro-2-methylphenyl)sulfanylmethyl]pyrrolidine | —— | C12H16FNS |
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—— | methyl (2R)-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]butanoate | —— | C12H13N3O3S |
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—— | (2R)-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]propanoic acid | —— | C10H9N3O3S |
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—— | (2R)-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]butanoic acid | —— | C11H11N3O3S |
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—— | (2S)-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]butanoic acid | —— | C11H11N3O3S |
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—— | 2-(2-Ethoxyethylsulfanyl)-5-pyridin-4-yl-1,3,4-oxadiazole | —— | C11H13N3O2S |
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—— | (2S)-N,N-dimethyl-3-oxo-2-[(5-pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]butanamide | —— | C13H14N4O3S |
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—— | 2-[(1S)-1-phenylethyl]sulfanyl-5-pyridin-4-yl-1,3,4-oxadiazole | —— | C15H13N3OS |
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—— | 4-[2-[(5-Pyridin-4-yl-1,3,4-oxadiazol-2-yl)sulfanyl]ethyl]morpholine | —— | C13H16N4O2S |
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