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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—— | 4-(benzylthio)pyridin-2-amine | —— | C12H12N2S |
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—— | 2-(benzylthio)-5-methyl-3-nitropyridine | —— | C13H12N2O2S |
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—— | 6-(benzylthio)nicotinonitrile | —— | C13H10N2S |
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—— | 5-(benzylthio)pyridin-2-amine | 1019484-60-6 | C12H12N2S |
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—— | 3-(benzylthio)pyridine-2-carbonitrile | —— | C13H10N2S |
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—— | 2-(benzylthio)-4-bromopyridine | —— | C12H10BrNS |
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—— | 4-(benzylthio)-2-fluoropyridine | —— | C12H10FNS |
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—— | 4-(benzylthio)-2-(trifluoromethyl)pyridine | —— | C13H10F3NS |
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—— | 8-(2,5-dimethoxy-phenylsulfanyl)-9-phenethyl-9H-purin-6-ylamine | —— | C21H21N5O2S |
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—— | (E)- and (Z)-1-phenyl-2-(benzylthio)-2-(phenylthio)ethylene | —— | C21H18S2 |
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—— | 3-(benzylsulfanyl-phenyl-methyl-sulfanyl)-4-trifluoromethylpyridine | —— | C20H16F3NS2 |
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—— | 3-benzylsulfanyl-4-trifluoromethylpyridine | —— | C13H10F3NS |
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—— | 6-(4-bromo-phenylylsulfanyl)-hexanoic acid methyl ester | —— | C13H17BrO2S |
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—— | (E)-2-iodo-3-phenylthio-2-propen-1-ol | —— | C9H9IOS |
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—— | 5,6-Dihydro-4-hydroxy-6-phenyl-6-(2-phenylethyl)-3-phenylthio-2H-pyran-2-one | —— | C25H22O3S |
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—— | 5-[(4-methylphenyl)sulfanylmethyl]-5-phenyl-3a,4,5,6-tetrahydro-2(3H)-pentalenone | —— | C22H22OS |
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—— | 2-allyl-4-methyl-2-phenylpent-4-enyl 4-methylphenyl sulfide | —— | C22H26S |
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—— | N4-benzyl-6-chloro-2-propylsulfanylpyrimidine-4,5-diamine | —— | C14H17ClN4S |
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—— | 2-ethoxycarbonyl-4-mesitylthio-2,5-dihydrofuran | —— | C16H20O3S |
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—— | 2-chloro-5-(methylthio)aniline hydrochloride | —— | C7H8ClNS*ClH |
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—— | (Z)-1-(1,2-bis(phenylthio)vinyl)cyclohexanol | —— | C20H22OS2 |
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—— | 1-phenylthio-2-(2,4,6-trimethylphenyl)ethyne | —— | C17H16S |
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—— | (Z)-1,2-bis(phenylthio)-1-hexene | —— | C18H20S2 |
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—— | 2,3-bis-phenylsulfanyl-propionic acid methyl ester | —— | C16H16O2S2 |
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—— | 2,2-dimethyl-4-(phenylthiomethyl)-1,3-dioxolane | —— | C12H16O2S |
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—— | 1-phenylthio-2-triethylsilylethyne | —— | C14H20SSi |
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—— | 2-(naphthalen-2-yl)-3-(phenylthio)imidazo[1,2-a]pyridine | —— | C23H16N2S |
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—— | 2-phenyl-5-(phenylthio)thiophene | —— | C16H12S2 |
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—— | (16,16,16-trifluoro-3-hydroxy-1-hexadecenyl)phenyl sulfide | —— | C44H64F6O2S |
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—— | 2,5-Bis-phenylthio-1-benzyloxymethyl-4-methylimidazole | —— | C24H22N2OS2 |
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—— | 1-benzyloxymethyl-4-methyl-5-phenylthioimidazole | —— | C18H18N2OS |
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—— | 2-(m-tolylthio)phenol | —— | C13H12OS |
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—— | 5-bromo-3-(phenylsulfanyl)-1H-pyrrolo[2,3-b]pyridine | —— | C13H9BrN2S |
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—— | 5-bromo-2-methyl-3-(phenylthio)-1H-indole | —— | C15H12BrNS |
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—— | 3-phenylsulfanyl-7-(2-pyrrolidin-1-yl-ethoxy)-1H-indole | —— | C20H22N2OS |
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—— | 5-chloro-2-methyl-3-(phenylthio)-1H-indole | —— | C15H12ClNS |
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—— | 3,5-dichlorophenyl phenyl sulfide | —— | C12H8Cl2S |
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—— | 3,5-dimethylphenyl 2-methyl-1-butyl sulfide | —— | C13H20S |
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—— | 3,5-dimethylphenyl dodecyl sulfide | —— | C20H34S |
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—— | phenyl 4,6-di-O-acetyl-2,3-dideoxy-1-thio-D-erythro-hex-2-enopyranoside | —— | C16H18O5S |
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—— | pent-1-yn-1-yl(phenyl)sulfane | —— | C11H12S |
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—— | 5-fluoro-3-(phenylthio)-1H-indole | —— | C14H10FNS |
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—— | 7-exo-(phenylmethyl)-7-(phenylthio)bicyclo[3.2.0]hept-2-en-6-one | —— | C20H18OS |
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—— | 3-methoxy-2-methyl-4-(phenylthio)cyclobuten-2-one | —— | C12H12O2S |
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—— | 7-Methyl-7-(phenylthio)bicyclo<3.2.0>-2-hepten-6-on | —— | C14H14OS |
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—— | 7-(phenylthio)bicyclo[3.2.0]hept-2-en-6-one | —— | C13H12OS |
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—— | 3-(phenylthio)butyronitrile | —— | C10H11NS |
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—— | ethyl 2-amino-5-(p-tolylthio)benzoate | —— | C16H17NO2S |
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—— | 2-Amino-2-thioxo-thioethansaeure-O-ethylester | —— | C4H7NOS2 |
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—— | <i>S</i>-decyl-<i>N</i>,<i>N</i>'-dimethyl-isothiourea | —— | C13H28N2S |
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