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-fluoroethyl)(4-fluorophenyl)sulfane | —— | C8H8F2S |
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—— | diethyl (4-fluorophenylthio)methylphosphonate | —— | C11H16FO3PS |
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—— | 4-ethoxycarbonylmethylthio-3-phenylsydnone | —— | C12H12N2O4S |
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—— | 4-fluorophenyl 2-ethylphenyl sulfide | —— | C14H13FS |
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—— | 4-fluorophenyl 2-tolyl sulfide | —— | C13H11FS |
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—— | 4-fluorophenyl 3-ethylphenyl sulfide | —— | C14H13FS |
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—— | 4-fluorophenyl 3-tolyl sulfide | —— | C13H11FS |
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—— | 4-fluorophenyl 4-ethylphenyl sulfide | —— | C14H13FS |
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—— | (RS<sub>S</sub>,RS<sub>β</sub>,RS<sub>α</sub>)-N-tert-butyl-N-(1-tert-butyl-2-ethylsulfinylpropyl)hydroxylamine | —— | C13H29NO2S |
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—— | 1-chloro-1-(ethylsulfinyl)ethyl ethane | —— | C4H9ClOS |
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—— | 2-isopropyl-4,6-dichloro-5-ethylthiopyrimidine | —— | C9H12Cl2N2S |
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—— | O-Propyl propylcarbamothioate | —— | C7H15NOS |
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—— | (+/-)-n-propyl-thiocarbamic acid O((E)-1-methyl-but-2-enyl) ester | —— | C9H17NOS |
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—— | (+/-)-n-propyl-thiocarbamic acid O-(cyclohex-2-enyl) ester | —— | C10H17NOS |
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—— | 2,8-dimethyl-5,5-bis(methylthio)-7-(trimethylsiloxy)nona-1,8-dien-3-ol | —— | C16H32O2S2Si |
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—— | 2,8-dimethyl-5,5-bis(methylthio)nona-1,8-diene-3,7-diol | —— | C13H24O2S2 |
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—— | (4-bromophenyl)(but-3-yn-1-yl)sulfane | —— | C10H9BrS |
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—— | methyl(2-(o-tolylethynyl)phenyl)sulfane | —— | C16H14S |
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—— | but-3-yn-1-yl(4-fluorophenyl)sulfane | —— | C10H9FS |
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—— | 4-chloro-2-[(trifluoromethyl)thio]aniline | —— | C7H5ClF3NS |
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—— | (E)-N'-(2-hydroxybenzylidene)-2-((5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)thio)acetohydrazide | 1523215-49-7 | C16H13N5O3S |
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—— | 1,3-bis(cyclohexylmethyl)thiourea | —— | C15H28N2S |
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—— | 13-(3-hydroxyphenyl)-12H-thiopyrano[2,3-b:6,5-b']bis(thiochromene)-12,14(13H)-dione | —— | C25H14O3S3 |
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—— | tert.-octylthiomethylamine | —— | C9H21NS |
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—— | 2-methyl-4-phenyl-4-thiophenyl-2-butanol | —— | C17H20OS |
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—— | <i>N</i>'-allyl-<i>N</i>-hydroxy-<i>N</i>-methyl-thiourea | —— | C5H10N2OS |
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—— | N-methyl-N-thiobutyrylhydroxylamine | —— | C5H11NOS |
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—— | (4-fluorophenyl)(prop-2-yn-1-yl)sulfane | —— | C9H7FS |
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—— | N-methyl-N-thiopivaloylhydroxamic acid | —— | C6H13NOS |
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—— | 1-((4-bromophenyl)thio)-2-methylpropan-2-ol | —— | C10H13BrOS |
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—— | 7-Bromo-6-methyl-1-oxa-4-thiaspiro[4.5]dec-6-ene | —— | C9H13BrOS |
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—— | 4-(4,7,7-trimethyl-9-(2-methylpiperidin-1-yl)-7,8-dihydro-6H-benzo[b]pyrimido[5,4-e][1,4]thiazin-2-yl)morpholine | —— | C23H33N5OS |
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—— | 4-(4,7,7-trimethyl-9-(pyrrolidin-1-yl)-7,8-dihydro-6H-benzo[b]pyrimido[5,4-e][1,4]thiazin-2-yl)morpholine | —— | C21H29N5OS |
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—— | 1,4-dithia-7-aza-spiro[4.4]nonane-6,8-dione | —— | C6H7NO2S2 |
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—— | 2-ethyl-2-pentyl-1,3-dithiolane | —— | C10H20S2 |
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—— | [4-(4-chlorophenylsulfanyl)phenyl]-(3,4,5,6-tetrahydropyridin-2-yl)amine hydrochloride | —— | C17H17ClN2S*ClH |
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—— | 2-methyl-1-(1-methylethyl)propyl 1,4-dithiaspiro[4.5]decane-8-carboxylate | —— | C16H28O2S2 |
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—— | 3-butyl-1,5,3-dithiazepane | —— | C8H17NS2 |
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—— | methyl 8-(2-heptyl-[1,3]dithiolan-2-yl)-octanoate | —— | C19H36O2S2 |
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—— | ethyl 1,4-dithiaspiro[4.5]decane-8-carboxylate | —— | C11H18O2S2 |
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—— | <i>N</i>,<i>N</i>',<i>N</i>'',<i>N</i>'''-tetraethyl-<i>S,S'</i>-ethanediyl-bis-isothiourea | —— | C12H26N4S2 |
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—— | spiro(benzo-1,5-dithiepan-3,1'-cyclobutane) | —— | C12H14S2 |
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—— | 2-ethoxy-2,3-dihydro-benzo[1,4]dithiin | —— | C10H12OS2 |
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—— | 2,2'-(o-Phenylenedithio)bis(3,5,6-trichloropyridine) | —— | C16H6Cl6N2S2 |
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—— | N-[(2,3-Dihydro-1,4-benzodithiin-2-yl)methyl]acetamide | —— | C11H13NOS2 |
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—— | ethyl 2-(1,4-benzodithiin-2-yl)-2-methoxyiminoacetate | —— | C13H13NO3S2 |
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—— | <i>N</i>,<i>N</i>'-diethyl-<i>N</i>,<i>N</i>'-dimethyl-thiourea | —— | C7H16N2S |
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—— | tribenzo[b,f,h][1,4]dithiecin | —— | C20H16S2 |
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—— | trans-2-(ethoxycarbonyl)-3-phenyl-1,4-benzodithiene | —— | C17H16O2S2 |
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—— | 4-(3-hydroxyphenylthio)-2,5-xylidine | —— | C14H15NOS |
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