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-(4-Chlorophenyl)-5-[(5-phenyl-1,2-oxazol-3-yl)methylsulfanyl]-1,3,4-oxadiazole | —— | C18H12ClN3O2S |
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—— | (3S)-3-prop-2-ynylsulfonylbutan-2-one | —— | C7H10O3S |
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—— | 2-[[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-methyl-N-(thiophen-3-ylmethyl)acetamide | —— | C16H14ClN3O2S2 |
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—— | 2-[[5-(4-chlorophenyl)-1,3,4-oxadiazol-2-yl]sulfanyl]-N-[(2S)-2-ethylhexyl]acetamide | —— | C18H24ClN3O2S |
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—— | 2-methoxyethyl (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C9H14O5S |
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—— | butyl (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | cyclohexyl (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C12H18O4S |
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—— | propan-2-yl (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C9H14O4S |
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—— | [(2S)-butan-2-yl] 2-prop-2-ynylsulfonylacetate | —— | C9H14O4S |
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—— | butyl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | N-[(2S)-butan-2-yl]-2-prop-2-ynylsulfonylacetamide | —— | C9H15NO3S |
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—— | [(2S)-1-methoxypropan-2-yl] 2-prop-2-ynylsulfonylacetate | —— | C9H14O5S |
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—— | [(2R)-1-methoxypropan-2-yl] 2-prop-2-ynylsulfonylacetate | —— | C9H14O5S |
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—— | methyl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C7H10O4S |
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—— | rac-(1R,3R)-2,2-dimethyl-3-[4-(methylsulfanyl)phenyl]cyclopropane-1-carboxylic acid | —— | C13H16O2S |
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—— | (2S)-3-prop-2-ynylsulfonylpropane-1,2-diol | —— | C6H10O4S |
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—— | (2R)-3-prop-2-ynylsulfonylpropane-1,2-diol | —— | C6H10O4S |
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—— | [(2R)-butan-2-yl] (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | propyl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C9H14O4S |
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—— | propan-2-yl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C9H14O4S |
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—— | 2-methoxyethyl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C9H14O5S |
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—— | N-[(2R)-butan-2-yl]-2-prop-2-ynylsulfonylacetamide | —— | C9H15NO3S |
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—— | 3-methylbutyl (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C11H18O4S |
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—— | [(2R)-butan-2-yl] (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | [(2S)-butan-2-yl] (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | 2-methylpropyl (2S)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | [(2S)-butan-2-yl] (2R)-2-prop-2-ynylsulfonylpropanoate | —— | C10H16O4S |
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—— | (1S,3R)-2,2-dimethyl-3-(4-methylsulfanylphenyl)cyclopropane-1-carboxylic acid | —— | C13H16O2S |
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—— | (1R,3S)-2,2-dimethyl-3-(4-methylsulfanylphenyl)cyclopropane-1-carboxylic acid | —— | C13H16O2S |
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—— | (2S)-N-cyclopentyl-3-methyl-2-[(4-methyl-5-morpholin-4-yl-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C17H29N5O2S |
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—— | (2R)-N-cyclopentyl-3-methyl-2-[(4-methyl-5-morpholin-4-yl-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C17H29N5O2S |
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—— | 5-(5,6-dimethylthieno[2,3-d]pyrimidin-4-yl)sulfanyl-N-phenyl-1,3,4-thiadiazol-2-amine | —— | C16H13N5S3 |
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—— | N-phenyl-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C14H9N5S3 |
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—— | 2-[(5-Anilino-1,3,4-thiadiazol-2-yl)sulfanyl]-5-nitrobenzonitrile | —— | C15H9N5O2S2 |
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—— | N-(4-methoxyphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C15H11N5OS3 |
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—— | 2-[[4-ethyl-5-(furan-2-yl)-1,2,4-triazol-3-yl]sulfanyl]-N-[2-(thiophen-2-ylmethylsulfanyl)ethyl]acetamide | —— | C17H20N4O2S3 |
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—— | N-(2,4-dimethylphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C16H13N5S3 |
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—— | 5-(2-nitrophenyl)sulfanyl-N-phenyl-1,3,4-thiadiazol-2-amine | —— | C14H10N4O2S2 |
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—— | N-(2-methoxyphenyl)-5-(7-thia-9,11-diazatricyclo[6.4.0.02,6]dodeca-1(8),2(6),9,11-tetraen-12-ylsulfanyl)-1,3,4-thiadiazol-2-amine | —— | C18H15N5OS3 |
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—— | N-(4-methoxyphenyl)-5-(2-nitrophenyl)sulfanyl-1,3,4-thiadiazol-2-amine | —— | C15H12N4O3S2 |
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—— | N-(2,3-dimethylphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C16H13N5S3 |
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—— | 2-[[5-(4-Methylanilino)-1,3,4-thiadiazol-2-yl]sulfanyl]-5-nitrobenzonitrile | —— | C16H11N5O2S2 |
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—— | N-(3,4-dimethylphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C16H13N5S3 |
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—— | N-(2-methoxyphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C15H11N5OS3 |
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—— | 5-(5,6-dimethylthieno[2,3-d]pyrimidin-4-yl)sulfanyl-N-(2-methoxyphenyl)-1,3,4-thiadiazol-2-amine | —— | C17H15N5OS3 |
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—— | 2-[[5-(3-Methylanilino)-1,3,4-thiadiazol-2-yl]sulfanyl]-5-nitrobenzonitrile | —— | C16H11N5O2S2 |
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—— | N-(2-methoxyphenyl)-5-(2-nitrophenyl)sulfanyl-1,3,4-thiadiazol-2-amine | —— | C15H12N4O3S2 |
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—— | 2-(4-bromophenyl)sulfanyl-N-[2-(thiophen-2-ylmethylsulfanyl)ethyl]acetamide | —— | C15H16BrNOS3 |
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—— | N-(4-methylphenyl)-5-thieno[2,3-d]pyrimidin-4-ylsulfanyl-1,3,4-thiadiazol-2-amine | —— | C15H11N5S3 |
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—— | 2-[[5-[[(3R)-1,1-dioxothiolan-3-yl]methyl]-4-methyl-1,2,4-triazol-3-yl]sulfanyl]-N-[(2-fluorophenyl)methyl]acetamide | —— | C17H21FN4O3S2 |
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