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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—— | 5-methoxy-2-((4-methoxyphenyl)thio)phenol | —— | C14H14O3S |
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—— | 4-(4-methoxyphenylthio)quinazoline | —— | C15H12N2OS |
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—— | 4-cyanophenyl-2-pyrimidinylthioether | —— | C11H7N3S |
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—— | 4-(2-methyl-1,3-dithian-2-yl)butan-2-one | —— | C9H16OS2 |
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—— | (3-fluorophenyl)(4-methoxyphenyl)sulfane | —— | C13H11FOS |
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—— | 4-chloro-N-(3-fluorophenyl)-6-[(4-methoxyphenyl)thio]-1,3,5-triazin-2-amine | —— | C16H12ClFN4OS |
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—— | tert-butyl 6-chloro-3-(4-methoxy-phenylsulfanyl)-2-pyridinecarboxylate | —— | C17H18ClNO3S |
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—— | 2-((4-methoxyphenyl)thio)-1,3-benzoselenazole | —— | C14H11NOSSe |
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—— | methyl 3-(4-nitrophenylsulfanyl)benzoate | —— | C14H11NO4S |
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—— | 3-(4-methoxyphenyl)sulfanylbenzylamine | —— | C14H15NOS |
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—— | 5-(4-methoxyphenyl)sulfanylindole | —— | C15H13NOS |
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—— | 4-nitrophenyl 2-isopropylphenyl sulfide | —— | C15H15NO2S |
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—— | 3-[(4-methoxyphenyl)thio]-4-methylbenzoic acid | —— | C15H14O3S |
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—— | 3-chloro-5-methoxyphenyl 4-methoxyphenyl sulfide | —— | C14H13ClO2S |
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—— | 1-methoxy-4-(3-trifluoromethylphenylsulfanyl)-benzene | —— | C14H11F3OS |
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—— | 5-[(4-methoxyphenyl)sulfanyl]-9H-pyrimido[4,5-b]indole-2,4-diamine | —— | C17H15N5OS |
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—— | (4-methoxyphenyl)(2,3,5,6-tetrafluorophenyl)sulfane | —— | C13H8F4OS |
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—— | 2-isopropylphenyl 4-methoxyphenyl sulfide | —— | C16H18OS |
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—— | (3,4-dimethylphenyl)(4-methoxyphenyl)sulfane | —— | C15H16OS |
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—— | 3-(4-methoxyphenylthio)pyridine | —— | C12H11NOS |
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—— | (Z)-2-phenylseleno-1-(p-tolylthio)-1-octene | —— | C21H26SSe |
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—— | (Z)-1-phenylseleno-2-(p-tolylthio)-1-octene | —— | C21H26SSe |
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—— | 4-<<(3-Chlorophenyl)sulfanyl>methyl>piperidine hydrochloride | —— | C12H16ClNS*ClH |
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—— | 5-chloro-2-phenyl-1,4-benzodithiin | —— | C14H9ClS2 |
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—— | 3-(3-chlorophenylsulfanylmethyl)pyrrolidine | —— | C11H14ClNS |
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—— | 2-((3-cyano-4,6-dimethylpyridin-2-yl)thio)acetohydrazide | —— | C10H12N4OS |
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—— | 1-(tert-butyl)-3-((3-chlorophenyl)thio)-1H-pyrazolo[3,4-d]pyrimidin-4-amine | —— | C15H16ClN5S |
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—— | 3-(3-chlorophenylthio)-3-methylbutanoic acid | —— | C11H13ClO2S |
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—— | 4-(3-chloro-phenylsulfanyl)-<i>m</i>-phenylenediamine | —— | C12H11ClN2S |
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—— | 5-bromo-3-(p-tolylthio)-1H-indole | —— | C15H12BrNS |
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—— | (3R,4S)-4-(3-chlorophenylthiomethyl)-3-hydroxypyrrolidine hydrochloride | —— | C11H14ClNOS*ClH |
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—— | N-diaminomethylene-2-methyl-4-(3-chlorophenylthio)-5-methylsulfonylbenzamide | —— | C16H16ClN3O3S2 |
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—— | 1-chloro-2-(3-chlorobenzenethio)ethane | —— | C8H8Cl2S |
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—— | ethyl 4-(p-tolylthio)benzoate | —— | C16H16O2S |
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—— | 2-(p-tolylthio)benzo[d]oxazole | —— | C14H11NOS |
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—— | (3-chlorophenyl)(mesityl)sulfane | —— | C15H15ClS |
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—— | 2-phenyl-5-(4-methylphenylthio)-1,3,4-oxadiazole | —— | C15H12N2OS |
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—— | 2-{3-[(3-chlorophenyl)thio]but-1-yn-1-yl}-6-methylpyridine | —— | C16H14ClNS |
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—— | (E)-1,2-di(4-methylphenylthio)-1-octene | —— | C22H28S2 |
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—— | (Z)-1,2-bis[(4-methylphenyl)thio]hex-1-ene | —— | C20H24S2 |
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—— | 2-((3-chlorophenyl)thio)-1-phenylethanol | —— | C14H13ClOS |
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—— | 1-(p-tolylthio)-2-triethylsilylethyne | —— | C15H22SSi |
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—— | 2-{3-[(3-chlorophenyl)thio]prop-1-yn-1-yl}-6-methylpyridine | —— | C15H12ClNS |
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—— | 5-[(3-chlorophenyl)thio]-4-phenyl-1,2,3-thiadiazole | —— | C14H9ClN2S2 |
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—— | 1,3-bis(p-tolylthio)bicyclo[1.1.1]pentane | —— | C19H20S2 |
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—— | potassium {[(3-chlorophenyl)thio]methyl}trifluoroborate | —— | C7H6BClF3S*K |
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—— | 1-((3-chlorophenyl)thio)-2-phenylpropan-2-ol | —— | C15H15ClOS |
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—— | bicyclo[1.1.1]pent-1-yl(3-chlorophenyl)sulfane | —— | C11H11ClS |
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—— | 1-(2-chloro-pyridin-5-yl-methyl)-2-(1-nitro-2-(3-chloro-phenylthio)-ethylidene)imidazolidine | —— | C17H16Cl2N4O2S |
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—— | 3-(3-chlorophenylthio)-4-oxocyclohexaneacetic acid ethyl ester | —— | C16H19ClO3S |
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