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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—— | (2S)-1-(4-ethylpiperazin-1-yl)-2-[(5-ethylsulfanyl-1,3,4-thiadiazol-2-yl)sulfanyl]propan-1-one | —— | C13H22N4OS3 |
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—— | (2S)-2-[(4-methyl-5-morpholin-4-yl-1,2,4-triazol-3-yl)sulfanyl]-N-[(2S)-2-phenylpropyl]propanamide | —— | C19H27N5O2S |
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—— | ethyl 2-[[5-[(1R)-1-amino-3-methylbutyl]-1,3,4-oxadiazol-2-yl]sulfanyl]acetate | —— | C11H19N3O3S |
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—— | [(1R)-1-[5-(2-ethoxy-2-oxoethyl)sulfanyl-1,3,4-oxadiazol-2-yl]-3-methylbutyl]azanium | —— | C11H20N3O3S+ |
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—— | ethyl (1S,5R,6R)-5-hydroxy-1-(trifluoromethyl)spiro[2-oxa-7-thiabicyclo[3.2.1]octane-4,1'-cyclohexane]-6-carboxylate | —— | C15H21F3O4S |
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—— | N-(3-amino-3-sulfanylidenepropyl)-N-[(1S,2S)-2-methylcyclohexyl]acetamide | —— | C12H22N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-N-[(1S,2R)-2-methylcyclohexyl]propanamide | —— | C13H24N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-2,2,2-trifluoro-N-[(1R,2S)-2-methylcyclohexyl]acetamide | —— | C12H19F3N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-N-prop-2-enyladamantane-1-carboxamide | —— | C17H26N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-2,2-dimethyl-N-[(1S,2S)-2-methylcyclohexyl]propanamide | —— | C15H28N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-2-methyl-N-[(1S,2R)-2-methylcyclohexyl]propanamide | —— | C14H26N2OS |
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—— | N-(3-amino-3-sulfanylidenepropyl)-N-[(2R)-butan-2-yl]-3-cyclohexylpropanamide | —— | C16H30N2OS |
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—— | methyl (2R)-2-(2-aminophenyl)sulfanylbutanoate | —— | C11H15NO2S |
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—— | 2-methylpropyl (2R)-2-(2-aminophenyl)sulfanylpropanoate | —— | C13H19NO2S |
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—— | (8R,8aS)-6-amino-8-(4-methylsulfanylphenyl)-2-propan-2-yl-1,3,8,8a-tetrahydroisoquinoline-5,7,7-tricarbonitrile | —— | C22H23N5S |
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—— | propan-2-yl (2S)-2-(2-aminophenyl)sulfanylbutanoate | —— | C13H19NO2S |
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—— | propan-2-yl (2R)-2-(2-aminophenyl)sulfanylbutanoate | —— | C13H19NO2S |
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—— | propan-2-yl (2R)-2-(2-aminophenyl)sulfanylpropanoate | —— | C12H17NO2S |
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—— | (2S)-3-(2-aminophenyl)sulfanylpropane-1,2-diol | —— | C9H13NO2S |
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—— | [(2S)-butan-2-yl] (2R)-2-(2-aminophenyl)sulfanylpropanoate | —— | C13H19NO2S |
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—— | propyl (2R)-2-(2-aminophenyl)sulfanylbutanoate | —— | C13H19NO2S |
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—— | (2R)-4-(4-methylphenyl)sulfanyl-3-oxo-2-[5-(trifluoromethyl)pyridin-2-yl]butanenitrile | —— | C17H13F3N2OS |
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—— | (2S)-5-(4,6-dimethyl-2-methylsulfanylpyrimidin-5-yl)-3-oxo-2-pyridin-2-ylpentanenitrile | —— | C17H18N4OS |
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—— | N-[[(3S)-3-morpholin-4-ylthiolan-3-yl]methyl]-2-phenylsulfanylacetamide | —— | C17H24N2O2S2 |
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—— | (5R)-5-[[(4S,4aR,8aR)-2,4-diphenyl-4,4a,5,6,7,8-hexahydrothiochromen-8a-yl]sulfanylmethyl]-4,5-dihydro-1,3-thiazol-2-amine | —— | C25H28N2S3 |
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—— | (8R,8aS)-6-amino-2-ethyl-8-(4-methylsulfanylphenyl)-1,3,8,8a-tetrahydroisoquinoline-5,7,7-tricarbonitrile | —— | C21H21N5S |
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—— | 2-(4,6-dimethylpyrimidin-2-yl)sulfanyl-N-[(2S)-2-(4-methylpiperidin-1-yl)-2-thiophen-2-ylethyl]acetamide | —— | C20H28N4OS2 |
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—— | (4S,8Z)-2-amino-6-methyl-4-(4-methylsulfanylphenyl)-8-[(4-methylsulfanylphenyl)methylidene]-4,5,6,7-tetrahydropyrano[3,2-c]pyridin-6-ium-3-carbonitrile | —— | C25H26N3OS2+ |
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—— | ethyl (2R)-2-[(3,5-dioxo-2H-1,2,4-triazin-6-yl)sulfanyl]-3-oxobutanoate | —— | C9H11N3O5S |
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—— | (2Z,5R)-2-[(Z)-benzylidenehydrazinylidene]-5-[[4-(difluoromethylsulfanyl)phenyl]methyl]-1,3-thiazolidin-4-one | —— | C18H15F2N3OS2 |
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—— | (2Z,5R)-5-[[3-(difluoromethylsulfanyl)phenyl]methyl]-2-[(Z)-pyridin-2-ylmethylidenehydrazinylidene]-1,3-thiazolidin-4-one | —— | C17H14F2N4OS2 |
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—— | (2Z,5R)-5-[[4-(difluoromethylsulfanyl)phenyl]methyl]-2-[(Z)-pyridin-4-ylmethylidenehydrazinylidene]-1,3-thiazolidin-4-one | —— | C17H14F2N4OS2 |
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—— | (5S,6R,7R)-5-methyl-7-(4-methylphenyl)-2-oxo-3,5,6,7-tetrahydrothiopyrano[2,3-d][1,3]thiazole-6-carbaldehyde | —— | C15H15NO2S2 |
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—— | (Z)-N-[3-[(4-chlorophenyl)methylsulfanyl]-5-propyl-1,2,4-triazol-4-yl]-1-[(1R)-cyclohex-3-en-1-yl]methanimine | —— | C19H23ClN4S |
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—— | 2-[(4-fluorophenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C13H15FN3OS+ |
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—— | 2-(2-methylprop-2-enylsulfanyl)-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C10H16N3OS+ |
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—— | 2-[(2-chlorophenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C13H15ClN3OS+ |
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—— | (Z)-N-[3-[(4-bromophenyl)methylsulfanyl]-5-methyl-1,2,4-triazol-4-yl]-1-[(1R)-cyclohex-3-en-1-yl]methanimine | —— | C17H19BrN4S |
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—— | (Z)-1-[(1R)-cyclohex-3-en-1-yl]-N-[3-[(4-methylphenyl)methylsulfanyl]-1,2,4-triazol-4-yl]methanimine | —— | C17H20N4S |
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—— | 2-[(4-methylphenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C14H18N3OS+ |
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—— | 6-methyl-5-[[5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazol-2-yl]sulfanylmethyl]-1H-pyrimidine-2,4-dione | —— | C12H16N5O3S+ |
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—— | 2-[(3-methylphenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C14H18N3OS+ |
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—— | 2-[(2-methylphenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C14H18N3OS+ |
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—— | 2-[[5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazol-2-yl]sulfanyl]acetamide | —— | C8H13N4O2S+ |
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—— | 2-[(2-fluorophenyl)methylsulfanyl]-5-[(2S)-pyrrolidin-1-ium-2-yl]-1,3,4-oxadiazole | —— | C13H15FN3OS+ |
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—— | [(1S)-1-[5-[2-(dimethylamino)-2-oxoethyl]sulfanyl-1,3,4-oxadiazol-2-yl]-3-methylbutyl]azanium | —— | C11H21N4O2S+ |
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—— | 2-[(2S)-3-benzylsulfonyl-2-hydroxypropyl]sulfanyl-4,6-dimethylpyridine-3-carbonitrile | —— | C18H20N2O3S2 |
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—— | (3R)-3-(4,6-diaminopyrimidin-2-yl)sulfanylbutanenitrile | —— | C8H11N5S |
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—— | (1R,2R)-2-[(6-amino-4-oxo-1H-pyrimidin-2-yl)sulfanyl]cyclopentane-1-carbonitrile | —— | C10H12N4OS |
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—— | (1R,2S)-2-[(6-amino-4-oxo-1H-pyrimidin-2-yl)sulfanyl]cyclopentane-1-carbonitrile | —— | C10H12N4OS |
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