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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—— | 3-fluoro-2-methylthio-pyridine | —— | C6H6FNS |
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—— | 2,5-dimethylphenyl 4-methoxyphenyl sulfide | —— | C15H16OS |
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—— | 2-((4-methoxyphenyl)thio)phenol | —— | C13H12O2S |
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—— | thiocarbamic acid <i>O</i>-isopentyl ester | —— | C6H13NOS |
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—— | 2-((3,4-dimethoxyphenyl)thio)-6-nitrobenz[d]oxazole | —— | C15H12N2O5S |
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—— | 5-chloro-2-((3,4-dimethoxyphenyl)thio)benz[d]oxazole | —— | C15H12ClNO3S |
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—— | 3-hydroxy-1-methyl-5-methylthiopyrazole-4-carbonitrile | 35877-47-5 | C6H7N3OS |
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—— | 2-((3,4-dimethoxyphenyl)thio)-5-methylbenz[d]oxazole | —— | C16H15NO3S |
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—— | 2-((3,4-dimethoxyphenyl)thio)benz[d]oxazole | —— | C15H13NO3S |
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—— | 1-(2-isothiocyanatoethyl)adamantane | —— | C13H19NS |
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—— | 4-(2,3,4,5,6-pentafluorophenylthio)-1,2-dimethoxybenzene | —— | C14H9F5O2S |
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—— | 4-(2-hydroxy ethyl)-3-thiamorpholinone | —— | C5H9NO3S |
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—— | ethyl (2E)-3-[4-(isopropylamino)-6-methyl-2-(methylthio)pyrimidin-5-yl] acrylate | —— | C14H21N3O2S |
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—— | 4-hydroxymethyl-1,8-dihydroxy-3,6-dithiaoctane | —— | C7H16O3S2 |
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—— | 4-(5-(methylthio)-1,3,4-oxadiazol-2-yl)phenol | —— | C9H8N2O2S |
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—— | 6-chloro-N<sup>4</sup>-isopropyl-2-(propylthio)pyrimidine-4,5-diamine | —— | C10H17ClN4S |
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—— | 5,5-difluoro-3-thia-pentanol | —— | C4H8F2OS |
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—— | 2-[5-amino-4-cyano-2-(2′-hydroxyethylthio)-2-methylfuran-3(2H)-ylidene]malononitrile | —— | C11H10N4O2S |
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—— | 6,6-Dimethyl-3-((2-hydroxyethyl)thio)-1-(pyrid-2-yl)-4,5,6,7-tetrahydrobenzo[c]thiophen-4-one | —— | C17H19NO2S2 |
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—— | 4-amino-1-(tert-butyl)-1,6-bis[(2-hydroxyethyl)sulfanyl]-3-imino-1,3-dihydrofuro[3,4-c]pyridine-7-carbonitrile | —— | C16H22N4O3S2 |
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—— | 2-hydroxyethyl ethyldisulfide | —— | C4H10OS2 |
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—— | 2-(2-butyldisulfanyl)ethanol | —— | C6H14OS2 |
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—— | 2-((perfluoroethyl)thio)ethan-1-ol | —— | C4H5F5OS |
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—— | 2,2'-bis(2-hydroxyethylsulfinyl)diethyl ether | —— | C8H18O5S2 |
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—— | 2-(vinylthio)-1-methylimidazole | —— | C6H8N2S |
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—— | 3,4-dihydro-3-(1-methylethyl)-6-(methylthio)-1H-2,1,3-benzothiadiazine-2,2-dioxide | —— | C11H16N2O2S2 |
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—— | 4-aminophenylthioacetylcarbamoylfumagillol | —— | C25H34N2O6S |
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—— | (3-bromophenyl)(2-chloroethyl)sulfane | —— | C8H8BrClS |
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—— | 1,4,7,10-tetrathiacyclododec-2-ene-2,3-dicarbonitrile | —— | C10H12N2S4 |
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—— | 1,2-bis-(2-diethylamino-ethanesulfonyl)-ethane | —— | C14H32N2O4S2 |
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—— | 2-(benzylthio)-5-chloro-3-nitropyridine | —— | C12H9ClN2O2S |
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—— | 4-(benzo[d]thiazol-2-ylthio)-3-chloroaniline | —— | C13H9ClN2S2 |
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—— | 3-(4-methylthioanilino)-1,2-propanediol | —— | C10H15NO2S |
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—— | 1-(diethylcarbamoyl)-4-bromo-5-(2,5-dimethylphenylthio)pyrazole | —— | C16H20BrN3OS |
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—— | N-(4-(methylthio)benzylidene)-1-phenylmethanamine | —— | C15H15NS |
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—— | 4-Cyano-1-(dimethylsulfamoyl)-5-(2-methoxy-6-methylphenylthio)pyrazole | —— | C14H16N4O3S2 |
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—— | trans-1,7-bis(phenylthio)-4-oxa-6-hepten-2-ol | —— | C18H20O2S2 |
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—— | bis-[2-(2-hydroxy-ethylsulfanyl)-ethyl]-sulfoxide | —— | C8H18O3S3 |
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—— | 2-<<2-(2-hydroxyethoxy)ethoxy>methylthio>ethanol | —— | C7H16O4S |
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—— | <i>S</i>,<i>S</i>-bis-(2-hydroxy-ethyl)-sulfimide | —— | C4H11NO2S |
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—— | methyl(1-oxido-1λ<sup>4</sup>-thietan-1-ylidene)carbamate | —— | C5H9NO3S |
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—— | bis-mercaptodiethylsulphide | —— | C4H12S3 |
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—— | 5-chloro-2-((3,4,4-trifluorobut-3-en-1-yl)thio)thiazole | —— | C7H5ClF3NS2 |
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—— | bis(phenylthio)methyltributylstannane | —— | C25H38S2Sn |
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—— | methyl (E)-3-[(4-chlorophenyl)thio]but-2-enoate | —— | C11H11ClO2S |
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—— | methyl (E)-3-(p-tolylthio)but-2-enoate | —— | C12H14O2S |
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—— | N-methylthiosulfoxydimethyl | —— | C3H9NOS2 |
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—— | 4-(n-butylamino)-6-phenylpyrimido[4,5-b][1,4]benzothiazepine | —— | C21H20N4S |
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—— | ethyl (E)-3-[(4-chlorophenyl)thio]but-2-enoate | —— | C12H13ClO2S |
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—— | methyl (E)-3-[(4-fluorophenyl)thio]but-2-enoate | —— | C11H11FO2S |
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