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-Methylthio-6-(o-chlorophenyl)-5-oxo-2,5-dihydro-1,2,4-triazine | —— | C10H8ClN3OS |
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—— | 2-methyl-3-methylthio-6-(1-chlorophenyl)-5-oxo-2,5-dihydro-1,2,4-triazine | —— | C11H12ClN3OS |
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—— | (4-pyridylthio)acetic acid | —— | C6H5NO2S |
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—— | 3-(2-bromophenylsulfanyl)propylamine | —— | C9H12BrNS |
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—— | N-(3-bromopropyl)(phenylsulfanyl)acetamide | —— | C11H14BrNOS |
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—— | 3-[3-(caprylamino)propylthio]pyridine | —— | C16H28N2S |
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—— | S-(1-butyn-3-yl)-O-methyl xanthate | —— | C6H8OS2 |
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—— | 3-n-pentylthiopropanethiol | —— | C8H18S2 |
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—— | 1-(dimethyl(oxo)-λ<sup>6</sup>-sulfanylidene)propan-2-one | —— | C5H10O2S |
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—— | trimethyloxosulfonium chloride | —— | C3H9ClOS |
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—— | 2,2'-thiobis(6-t-butyl-4-ethylphenol) | 82100-95-6 | C24H34O2S |
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—— | O-thiocarbamoyl-L-lactic acid | —— | C4H7NO3S |
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—— | 3-methyl-N-(2-(phenylthio)ethyl)butanamide | —— | C13H19NOS |
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—— | 1-ethylthioperfluoro-2-methyl-1-cyclopentene | —— | C8H5F9S |
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—— | 2-mercapto-5-phenyl-1,3,4-oxadiazolyl-(Z)-2-(2-aminothiazol-4-yl)-2-methoxyimino acetate | —— | C14H11N5O3S2 |
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—— | carbon disulfide anion | —— | CS2 |
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—— | 5-(ortho-tolylthio)uracil | —— | C11H10N2O2S |
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—— | 9,9-bis(trifluoromethylsulfonyl)bicyclo[6.1.0]non-4-ene | —— | C11H12F6O4S2 |
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—— | 6-amino-7-cyano-2-hydroxymethyl-8-[(4-trifluoromethylthio)phenyl]-4,8-dihydropyrano[3,2-b]pyran-4-one | —— | C17H11F3N2O4S |
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—— | phenyl 4-bromo-2-butenyl sulfide | —— | C10H11BrS |
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—— | 4-((4-fluorophenyl)thio)-N-(3-morpholinopropyl)-3-nitrobenzamide | —— | C20H22FN3O4S |
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—— | 3-chloro-2,5-dihydro-1,4-benzothiazepine | —— | C9H8ClNS |
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—— | 3-morpholino-N-(2-(phenylthio)ethyl)propan-1-amine | —— | C15H24N2OS |
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—— | 4-(methylthio)-N-octylaniline | —— | C15H25NS |
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—— | methyl 3-(2-(methylthio)phenyl)propiolate | —— | C11H10O2S |
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—— | O-methyl S-(pyridin-2-yl)carbonothioate | —— | C7H7NO2S |
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—— | 3-t-butyl-5-(methylsulfonylmethylthio)-1H-1,2,4-triazole | —— | C8H15N3O2S2 |
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—— | (4S,5S)-2-ethyl-4-hydroxymethyl-5-[4-(methylthio)phenyl]-2-oxazoline | —— | C13H17NO2S |
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—— | 1-methyl-5-(3-propionylpropyl)thio-1,2,3,4-tetrazole | —— | C8H14N4OS |
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—— | 2,4-diethyl-6-(phenylthio)pyrimidine | —— | C14H16N2S |
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—— | 2-benzylthio-7-chloro-5H-1,3,4-thiadiazolo[3,2-a]pyrimidin-5-one | —— | C12H8ClN3OS2 |
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—— | dimethyl-(2-methylsulfanyl-pyridin-4-yl)-amine | —— | C8H12N2S |
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—— | 4-(decyl)pyridine | —— | C15H25NS |
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—— | decyl 2-pyridyl sulfide | —— | C15H25NS |
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—— | O-decyl S-ethyl carbonothioate | —— | C13H26O2S |
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—— | 4,4,5,5-tetrafluoro-5-(phenylthio)pentanenitrile | —— | C11H9F4NS |
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—— | 19S-curacin A | —— | C23H35NOS |
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—— | 15,16-dihydrocuracin A | —— | C23H37NOS |
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—— | curacin B | —— | C23H35NOS |
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—— | 7-hydroxy-4a,6-dimethyl-2H,3H,4aH-furo[2,3-b]thiazine | —— | C8H11NO2S |
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—— | 2-(2-aminoethylthio)-4-(pyrrolidin-1-yl)pyridine-3-carbonitrile | —— | C12H16N4S |
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—— | 7-sulfamoyl-3,4-dihydrothieno[3,2-f]-1,4-thiazepin-5(2H)-one | —— | C7H8N2O3S3 |
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—— | 7-(1,3-benzothiazol-2-ylthio)-4,6-dinitro-2,1,3-benzoxadiazole 1-oxide | —— | C13H5N5O6S2 |
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—— | 2-((2-chloro-4-nitrophenyl)thio)benzo[d]thiazole | —— | C13H7ClN2O2S2 |
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—— | 2-((4-bromophenyl)thio)benzo[d]thiazole | —— | C13H8BrNS2 |
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—— | 2-((4-methoxyphenyl)thio)benzo[d]thiazole | —— | C14H11NOS2 |
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—— | ethyl [(2-amino-6-methylpyrimidin-4-yl)sulfanyl]acetate | —— | C9H13N3O2S |
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—— | 1,2-bis-[4-amino-5-carboethoxymethylthio-4H-(1,2,4-triazol-3-yl)]ethane | —— | C14H22N8O4S2 |
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—— | 3-(5-(pyridin-4-yl)-1,3,4-thiadiazol-2-ylthio)-N-benzylpropanamide | —— | C17H16N4OS2 |
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—— | ethyl 2-((5,6-di-p-tolyl-1,2,4-triazin-3-yl)thio)acetate | —— | C21H21N3O2S |
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