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-(tert-Butyldimethylsilyloxy)-2-phenylsulphanylphenoxy]diethoxyphosphane | —— | C22H33O4PSSi |
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—— | tert-butylthiomethanol | —— | C5H12OS |
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—— | 3-tert-butylsulfanyl-1,2,4-triazine | —— | C7H11N3S |
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—— | tert-butyl isoamyl sulfide | —— | C9H20S |
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—— | 1,2,4,5-tetrakis(n-dodecylthio)benzene | —— | C54H102S4 |
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—— | 1,2,4,5-tetrakis(n-octylthio)benzene | —— | C38H70S4 |
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—— | ethyl 2-bromo-2-methyldithiopropionate | —— | C6H11BrS2 |
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—— | (E)-4-(tert-butylthio)-4-octene | —— | C12H24S |
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—— | 6-(tert-butyldisulfanyl)hexan-1-ol | —— | C10H22OS2 |
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—— | 4-(1-hydroxyethyl)phenyl 2-methyl-2-propyl sulfide | —— | C12H18OS |
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—— | 2,5-dimethylphenyl 2-methyl-2-propyl sulfide | —— | C12H18S |
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—— | 3-(tert-butylthio)-2-chloroaniline | —— | C10H14ClNS |
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—— | n-Butyl tert-butyl disulfide | —— | C8H18S2 |
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—— | 4-phenylthio-2-phenyltetrahydro-2H-pyran | —— | C17H18OS |
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—— | 4-(p-tolylthio)-tetrahydro-2-p-tolyl-2H-pyran | —— | C19H22OS |
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—— | 4-(4-chlorophenylthio)-2-(4-chlorophenyl)tetrahydro-2H-pyran | —— | C17H16Cl2OS |
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—— | {3-[5-(3,5-dichloro-phenylsulfanyl)-4-isopropyl-1-pyridin-4-ylmethyl-1H-imidazol-2-ylmethoxycarbonylamino]-propyl}-phosphonic acid diethyl ester | —— | C27H35Cl2N4O5PS |
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—— | ethyl [3-(3-phenethylaminophenylsulphanyl)phenyl]acetate | —— | C24H25NO2S |
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—— | ethyl [3-(3-aminophenylsulphanyl)phenyl]acetate | —— | C16H17NO2S |
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—— | 6-amino-4-benzyl-2-methylsulfanylpyridine-3,5-dicarbonitrile | —— | C15H12N4S |
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—— | N-[5-(3-trifluoromethylphenylthio)thien-2-ylethyl]hydroxylamine | —— | C13H12F3NOS2 |
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—— | 1-Hydroxy-1-[5-(3-trifluoromethylphenylthio)thien-2-ylethyl]-urea | —— | C14H13F3N2O2S2 |
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—— | (2-methylsulfanylphenyl)triethylsilane | —— | C13H22SSi |
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—— | N-hydroxy-N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]urea | —— | C16H14F2N2O2S |
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—— | N-[3-[2-(4-fluorophenylthio)-6-fluorophenyl]prop-2-enyl]hydroxylamine | —— | C15H13F2NOS |
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—— | ferrocenylphenyl sulfide | —— | C16H14FeS |
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—— | 1-hydroxy-1-[5-(4-chlorophenylthio)thien-2-ylmethyl]urea | —— | C12H11ClN2O2S2 |
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—— | 3-phenylthiocyclopentanone oxime | —— | C11H13NOS |
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—— | 6-methyl-3-(phenylthio)pyrido[2,3-b]pyrazin-7-amine | —— | C14H12N4S |
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—— | 2-(4-chlorophenylthio)-2-phenylethanol | —— | C14H13ClOS |
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—— | (1R,6S,7R,8R)-6-n-butylthio-7,8-bishydroxymethylbicyclo[4.2.0]octane | —— | C14H26O2S |
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—— | barium bis(dodecyl mercaptide) | —— | Ba*2C12H25S |
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—— | dimethyl(1-phenylthio)cyclopropylsilane | —— | C11H16SSi |
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—— | sec-butyl 4,9-dihydrothieno[3,2-b][4,1]benzothiazepin-9-ylacetate | —— | C17H19NO2S2 |
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—— | 1-phenyl-2-(2-pyridylsulfanyl)ethanol | —— | C13H13NOS |
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—— | 2-((2-methylfuran-3-yl)thio)-1-phenylethan-1-ol | —— | C13H14O2S |
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—— | 2-((4-bromophenyl)thio)-1-phenylethanol | —— | C14H13BrOS |
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—— | O-isobutanoyl S-methyl thiocarbonate | —— | C6H10O3S |
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—— | 5,6-Dihydro-4H-4-hydroxymethylthieno[2,3-b]thiopyran | —— | C8H10OS2 |
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—— | 8-hydroxy-5,6,7,8-tetrahydrothieno[3,2-b]thiepin | —— | C8H10OS2 |
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—— | 5,6-dihydro-4H-4-(2-methoxyethoxymethoxy)thieno[2,3-b]thiopyran | —— | C11H16O3S2 |
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—— | 3-phenylthio-1,2,4-dithiazole-5-one | —— | C8H9NS2 |
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—— | 1,2-dithiobenzene | —— | C6H4S2 |
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—— | 2-(pyridin-4-ylsulfanyl)ethanol | —— | C7H9NOS |
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—— | 2-(pyridin-3-ylsulfanyl)ethanol | —— | C7H9NOS |
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—— | 2-(2,6-dimethyl phenylthio) 1-hydroxyethane | 65320-76-5 | C10H14OS |
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—— | 2-<5-(trifluoromethyl)pyridin-2-ylsulfanyl>ethanol | —— | C8H8F3NOS |
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—— | 1,1-bis-dimethylthiocarbamoylsulfanyl-acetone | —— | C9H16N2OS4 |
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—— | 1,1-bis(butylthio)-2-propanone | —— | C11H22OS2 |
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—— | (4,4-dimethylpentyl)(ethyl)sulfane | —— | C9H20S |
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