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-(2-(4-Chlorophenylthio)ethyl)-1,1,2-tribromocyclopropane | —— | C11H10Br3ClS |
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—— | 5-[(4-chlorophenyl)sulfanyl]-9H-pyrimido[4,5-b]indole-2,4-diamine | —— | C16H12ClN5S |
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—— | 3-((4-chlorophenyl)thio)-2-methyl-1H-indole | —— | C15H12ClNS |
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—— | (E)-1-(p-(chlorophenyl)thio)-1-dodecene | —— | C18H27ClS |
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—— | 1-(4-chlorophenylsulfanyl)-3-isopropoxypropan-2-ol | —— | C12H17ClO2S |
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—— | (Z)-4-(4-bromophenyl)-5-(((4-chlorophenyl)thio)methylene)-1,5-dihydro-2H-pyrrol-2-one | —— | C17H11BrClNOS |
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—— | (4-chlorophenyl)(2,3,5,6-tetrafluorophenyl)sulfane | —— | C12H5ClF4S |
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—— | 6-chloro-8-[4-(chlorophenyl)thio]-2-methyl-3-nitroimidazo[1,2-a]pyridine | —— | C14H9Cl2N3O2S |
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—— | (R)-2-(((4-chlorophenyl)thio)methyl)oxirane | —— | C9H9ClOS |
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—— | (4-chlorophenyl)(3-methoxyphenyl)sulfane | —— | C13H11ClOS |
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—— | 3-((4-chlorophenyl)thio)phenol | —— | C12H9ClOS |
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—— | 1-((4-chlorophenyl)thio)-2-methylpropan-2-ol | —— | C10H13ClOS |
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—— | 2,4-bis[(4-chlorophenyl)thio]-1-nitrobenzene | —— | C18H11Cl2NO2S2 |
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—— | ethyl 2-((4-chlorophenyl)thio)hexanoate | —— | C14H19ClO2S |
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—— | N-Boc-2-(4-chlorophenylthio)cyclohexylamine | —— | C17H24ClNO2S |
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—— | (4-chlorophenyl)(4-(trifluoromethyl)phenyl)sulfane | —— | C13H8ClF3S |
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—— | 4-((4-chlorophenyl)thio)-4-phenylbutan-2-one | —— | C16H15ClOS |
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—— | (4-chlorophenyl)(2-fluoroethyl)sulfane | —— | C8H8ClFS |
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—— | 5-[(p-chlorophenyl)thio]-3,4-dipropyl-5H-furan-2-one | —— | C16H19ClO2S |
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—— | 3-((4-chlorophenyl)thio)-1H-pyrrolo[2,3-b]pyridine | —— | C13H9ClN2S |
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—— | S-(4-chlorophenyl) tert-butylcarbamothioate | —— | C11H14ClNOS |
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—— | di(3-nitrilphenyl)sulfide | —— | C14H8N2S |
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—— | 4-chloro-N-[4-(methylthio)phenyl]benzenecarboximidamide | —— | C14H13ClN2S |
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—— | GCD-189 | 444889-02-5 | C15H18N5O5PS |
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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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