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-hydroxy-3-[(4-methylphenyl)sulfanyl]pent-3-en-2-one | —— | C12H14O2S |
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—— | (4-(tert-butyl)phenyl)(p-tolyl)sulfane | —— | C17H20S |
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—— | 5-(p-tolylthio)pyrimidine | —— | C11H10N2S |
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—— | (Z)-(1,1,1,4,4,4-hexafluorobut-2-en-2-yl)(p-tolyl)sulfane | —— | C11H8F6S |
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—— | 3-bromo-4-(p-tolylthio)pyridine | —— | C12H10BrNS |
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—— | 5-(4-tolyl)thio-6-chlorouracil | —— | C11H9ClN2O2S |
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—— | 1-(2-methyl-5-(phenyl(p-tolylthio)methyl)furan-3-yl)ethan-1-one | —— | C21H20O2S |
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—— | 6-methyl-5-(p-tolylthio)pyrimidine-2,4(1H,3H)-dione | —— | C12H12N2O2S |
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—— | 2-(p-tolylthio)benzonitrile | —— | C14H11NS |
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—— | 2,6-dimethyl-4-(p-tolylthio)aniline | —— | C15H17NS |
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—— | (S)-2-[bis(4-methylphenylthio)methyl]pyrrolidine | —— | C19H23NS2 |
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—— | (4-chlorophenethyl)(p-tolyl)sulfane | —— | C15H15ClS |
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—— | 1-(4-methylphenylthio)butan-2-ol | —— | C11H16OS |
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—— | (3,5-dimethyl phenyl) (p-tolyl)sulfane | —— | C15H16S |
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—— | 2-methyl-3-(p-tolylthio)-1H-indole | —— | C16H15NS |
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—— | 2,8-dimethyl-6H,12H-dibenzo<b,f><1,5>dithiocin | —— | C16H16S2 |
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—— | 3-[(4-methylphenyl)thio]-1-propanethiol | —— | C10H14S2 |
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—— | 5,6-dihydrothiazolo[3.2-d]tetrazole | —— | C3H4N4S |
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—— | 3-ethyl-3-isothiocyanatooctane | —— | C11H21NS |
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—— | 1-bromo-4-methylthiobutane | —— | C5H11BrS |
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—— | 2-(4-(methylthio)-1H-pyrazol-1-yl)acetonitrile | —— | C6H7N3S |
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—— | 3-ethyl-3-isothiocyanatononane | —— | C12H23NS |
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—— | 3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-5-[(4-methylphenyl)sulfanyl]-1,2,4-thiadiazole | —— | C14H16N2O2S2 |
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—— | 3-phenethyl-5-(p-tolylthio)-1,2,4-thiadiazole | —— | C17H16N2S2 |
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—— | 3-(adamantan-1-yl)sulfanyl-1,2,4-thiadiazole-5-amine | —— | C12H17N3S2 |
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—— | 2,4-dimethylphenyl isopropyl sulfide | —— | C11H16S |
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—— | ethyl 2-(5-nitropyridine-2-sulfanyl)acetate | —— | C9H10N2O4S |
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—— | ethyl 2-(3,4-dimethylphenylsulfanyl)acetate | —— | C12H16O2S |
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—— | ethyl 2-((2,4-dimethylphenyl)thio)acetate | —— | C12H16O2S |
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—— | 1-ethyl-4-<(methylethyl)thio>benzene | —— | C11H16S |
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—— | ethyl 2-((3-fluorophenyl)thio)acetate | —— | C10H11FO2S |
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—— | S-ethyl O-(2-ethylhexyl) carbonothioate | —— | C11H22O2S |
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—— | 2-Ethyl-3-hydroxyisothioharnstoff | —— | C3H8N2OS |
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—— | 3-ethylsulfanyl-5,7-dihydro-[2]pyrindine-6,6-dicarboxylic acid dimethyl ester | —— | C14H17NO4S |
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—— | 2-[(t-Butyldimethylsilyloxy)methyl]-4-[(4-chlorophenylthio)-(2,5-difluorophenyl)methyl]-5-methylpyridine | —— | C26H30ClF2NOSSi |
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—— | 2-[(4-chlorophenylthio)(2,5-difluorophenyl)methyl]-6-(1,3-dioxolan-2-yl)pyridine | —— | C21H16ClF2NO2S |
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—— | 4-[(4-Chlorophenylthio)-(2,5-difluorophenyl)-methyl]-2-(1,3-dioxolan-2-yl)-5-fluoropyridine | —— | C21H15ClF3NO2S |
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—— | 2-[(4-Chlorophenylthio)-(2,5-difluorophenyl)methyl]-5-(1,3-dioxolan-2-yl)pyridine | —— | C21H16ClF2NO2S |
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—— | S-2-(4-aminobutylamino)ethyl 4-chlorophenyl sulfide | —— | C12H19ClN2S |
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—— | S-2-(3-aminopropylamino)ethyl 4-chlorophenyl sulfide | —— | C11H17ClN2S |
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—— | (E)-1-(4-chlorophenyl)sulfanyl-1-trimethylsilyl-1-octene | —— | C17H27ClSSi |
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—— | 3-((4-chlorophenyl)thio)dihydrofuran-2(3H)-one | —— | C10H9ClO2S |
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—— | 3-((4-chlorophenyl)thio)-5-methoxy-1H-indole | —— | C15H12ClNOS |
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—— | 1-butoxy-3-(4-chlorophenylthio)propan-2-ol | —— | C13H19ClO2S |
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—— | 3-difluoromethoxy-4-cyano-5-(p-chlorophenylthio)isothiazole | —— | C11H5ClF2N2OS2 |
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—— | 2-((4-chlorophenyl)thio)tetrahydro-2H-pyran | —— | C11H13ClOS |
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—— | 2-((4-chlorophenyl)thio)-1-(4-fluorophenyl)ethan-1-ol | —— | C14H12ClFOS |
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—— | methyl trans-4-[(4-c chlorophenyl)sulfanyl]cyclohexanecarboxylate | —— | C14H17ClO2S |
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—— | 4-chlorophenyl (E)-(4-(methylsulfinyl)but-3-en-1-yl)carbamodithioate | —— | C12H14ClNOS3 |
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—— | 2-((4-chlorophenyl)thio)-1,3-benzoselenazole | —— | C13H8ClNSSe |
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