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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—— | (2E)-2-(2,5,6,7,8,9-hexahydro-[1,2,4]triazolo[4,3-a]azepin-3-ylidene)-3-oxo-4-pyrimidin-2-ylsulfanylbutanenitrile | —— | C15H16N6OS |
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—— | (5E)-2-(4-fluorophenyl)imino-3-methyl-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C18H15FN2OS2 |
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—— | (5E)-2-(2-chlorophenyl)imino-3-(2-methylpropyl)-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C21H21ClN2OS2 |
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—— | (5E)-2-(2-chlorophenyl)imino-3-ethyl-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C19H17ClN2OS2 |
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—— | (5E)-2-(3-chlorophenyl)imino-3-ethyl-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C19H17ClN2OS2 |
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—— | (5E)-2-(2-fluorophenyl)imino-3-methyl-5-[(5-phenylsulfanylfuran-2-yl)methylidene]-1,3-thiazolidin-4-one | —— | C21H15FN2O2S2 |
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—— | (5E)-5-[(3-hydroxyphenyl)methylidene]-3-methyl-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C18H16N2O2S2 |
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—— | (5E)-3-methyl-5-[(5-methylfuran-2-yl)methylidene]-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C17H16N2O2S2 |
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—— | (5E)-2-(2-fluorophenyl)imino-3-methyl-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C18H15FN2OS2 |
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—— | (5E)-3-methyl-2-(3-methylsulfanylphenyl)imino-5-[(5-morpholin-4-ylfuran-2-yl)methylidene]-1,3-thiazolidin-4-one | —— | C20H21N3O3S2 |
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—— | (5E)-3-methyl-2-phenylimino-5-[(5-phenylsulfanylfuran-2-yl)methylidene]-1,3-thiazolidin-4-one | —— | C21H16N2O2S2 |
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—— | (5E)-5-(furan-2-ylmethylidene)-3-methyl-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C16H14N2O2S2 |
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—— | (5E)-5-benzylidene-3-methyl-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C18H16N2OS2 |
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—— | (5E)-3-ethyl-2-(4-methylphenyl)imino-5-[(4-methylsulfanylphenyl)methylidene]-1,3-thiazolidin-4-one | —— | C20H20N2OS2 |
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—— | (2R)-2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]propanoate | —— | C5H6N3O2S2- |
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—— | (5E)-5-[(4-chlorophenyl)methylidene]-3-methyl-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C18H15ClN2OS2 |
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—— | (5E)-3-methyl-5-[(4-methylphenyl)methylidene]-2-(3-methylsulfanylphenyl)imino-1,3-thiazolidin-4-one | —— | C19H18N2OS2 |
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—— | 3-[(4-Phenyl-1,3-thiazol-2-yl)sulfanyl]propanoate | —— | C12H10NO2S2- |
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—— | (2S)-2-[(4-amino-1,2,4-triazol-3-yl)sulfanyl]propanoic acid | —— | C5H8N4O2S |
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—— | 3-(Pyrimidin-2-ylsulfanyl)propanoic acid | 919466-99-2 | C7H8N2O2S |
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—— | [2-oxo-2-[[(1R)-1-phenylbutyl]amino]ethyl] 2-(2-fluorophenyl)sulfanylacetate | —— | C20H22FNO3S |
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—— | 3-[(4-Phenyl-5-sulfanylidene-1,3,4-thiadiazol-2-yl)sulfanyl]propanoate | —— | C11H9N2O2S3- |
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—— | [(2S)-1-oxo-1-(propan-2-ylamino)propan-2-yl] 2-(2,4-dimethylphenyl)sulfanylacetate | —— | C16H23NO3S |
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—— | (2S)-2-pyrimidin-2-ylsulfanylpropanoate | —— | C7H7N2O2S- |
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—— | (2S)-2-[(4-phenyl-1,3-thiazol-2-yl)sulfanyl]propanoate | —— | C12H10NO2S2- |
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—— | 2-[(3-Methylsulfanyl-1,2,4-thiadiazol-5-yl)sulfanyl]acetate | —— | C5H5N2O2S3- |
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—— | (2R)-2-[[5-(3-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9BrN2O3S |
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—— | (2S)-2-[[5-(4-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C11H8BrN2O3S- |
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—— | (2R)-2-[(4-methyl-1,3-thiazol-2-yl)sulfanyl]propanoate | —— | C7H8NO2S2- |
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—— | (2R)-2-[(4-phenyl-1,3-thiazol-2-yl)sulfanyl]-N-propan-2-ylpropanamide | —— | C15H18N2OS2 |
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—— | 2-[[5-(2,3-dimethylanilino)-1,3,4-thiadiazol-2-yl]sulfanyl]-N-(3-propan-2-yloxypropyl)acetamide | —— | C18H26N4O2S2 |
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—— | (2S)-2-[[5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9FN2O3S |
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—— | (2S)-2-[[5-(4-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9BrN2O3S |
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—— | (2R)-2-[(5-pyridin-2-yl-1,3,4-oxadiazol-2-yl)sulfanyl]propanoic acid | —— | C10H9N3O3S |
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—— | (2S)-2-[(4-phenyl-1,3-thiazol-2-yl)sulfanyl]propanoic acid | —— | C12H11NO2S2 |
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—— | (2R)-2-[[5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C11H8FN2O3S- |
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—— | 3-[[5-(2-Fluorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9FN2O3S |
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—— | (2S)-2-[(4-phenyl-1,3-thiazol-2-yl)sulfanyl]-N-propan-2-ylpropanamide | —— | C15H18N2OS2 |
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—— | 3-[[5-(Furan-2-yl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C9H7N2O4S- |
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—— | (2S)-2-[[5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C11H8FN2O3S- |
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—— | (2S)-2-[[5-(3-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9BrN2O3S |
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—— | 3-[(4-Phenyl-1,3-thiazol-2-yl)sulfanyl]propanoic acid | —— | C12H11NO2S2 |
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—— | (2R)-2-[(5-pyridin-3-yl-1,3,4-oxadiazol-2-yl)sulfanyl]propanoate | —— | C10H8N3O3S- |
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—— | (2R)-2-[[5-(4-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C11H8BrN2O3S- |
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—— | (2S)-2-[[5-(3-fluorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C11H9FN2O3S |
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—— | (2S)-2-[[5-(5-methyl-1,2-oxazol-3-yl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoic acid | —— | C9H9N3O4S |
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—— | 2-[(5-Benzyl-1,3,4-oxadiazol-2-yl)sulfanyl]acetate | —— | C11H9N2O3S- |
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—— | (2S)-2-[[5-(3-bromophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]propanoate | —— | C11H8BrN2O3S- |
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—— | (2S)-2-[(5-ethyl-1,3,4-oxadiazol-2-yl)sulfanyl]propanoate | —— | C7H9N2O3S- |
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—— | 2-[[5-(2,3-dimethylanilino)-1,3,4-thiadiazol-2-yl]sulfanyl]-N-methyl-N-[(3-methylthiophen-2-yl)methyl]acetamide | —— | C19H22N4OS3 |
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