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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—— | (R)-(3-oxo-2-propyl-2,3-dihydro-benzo[b]thiophen-2-yl)-acetic acid methyl ester | —— | C14H16O3S |
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—— | 2-((2-((dimethylamino)methyl)phenyl)thio)-5-fluoroaniline | —— | C15H17FN2S |
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—— | 2-methoxycarbonylmethyl-3-oxo-2,3-dihydrobenzo[b]thiophene-2-carboxylic acid methyl ester | —— | C13H12O5S |
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—— | 2-(2-dimethylaminomethyl-phenylthio)-5-(2-fluoroethyl)phenylamine | —— | C17H21FN2S |
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—— | 2-(2,4-dinitrophenylthio)benzoyl chloride | —— | C13H7ClN2O5S |
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—— | 2-[2-(dimethylaminomethyl)phenylthio]-5-fluoromethylphenylamine | —— | C16H19FN2S |
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—— | (R)-(3-oxo-2-phenethyl-2,3-dihydro-benzo[b]thiophen-2-yl)-acetic acid methyl ester | —— | C19H18O3S |
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—— | 3-hexyl-2,3-dihydrobenzo[e]1,4-oxathiepin-5-one | —— | C15H20O2S |
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—— | methyl 2,2-difluoro-2-(4-(methylthio)phenyl)acetate | —— | C10H10F2O2S |
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—— | 2-hexyl-2,3-dihydrobenzo[e]1,4-oxathiepin-5-one | —— | C15H20O2S |
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—— | p-(methylthiophenyl)trichlorosilane | —— | C7H7Cl3SSi |
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—— | 2-phenyl-2,3-dihydrobenzo[e]1,4-oxathiepin-5-one | —— | C15H12O2S |
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—— | (1S,2R)-5-bromo-6-(methylsulfanyl)cyclohexa-4,6-diene-1,2-diol | —— | C7H9BrO4S |
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—— | (+)-cyclohexyl methyl sulfoxide | —— | C7H14OS |
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—— | 4-(methylthio)phenethyl formate | —— | C10H12O2S |
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—— | isopropyl 5-(2-carboxyphenylthio)-2-furancarboxylate | —— | C15H14O5S |
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—— | propyl 5-(2-carboxyphenylthio)-2-furancarboxylate | —— | C15H14O5S |
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—— | 4-(methylsulfanyl)phenyl 4-tolyl sulfide | —— | C14H14S2 |
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—— | (4-(methylthio)phenyl)zinc(II) bromide | —— | C7H7BrSZn |
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—— | 1,2-bis[5'-(4''-methylsulfanylphenyl)-2'-methylthien-3'-yl]cyclopentene | —— | C29H28S4 |
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—— | 4H‐spiro[benzo[d][1,3]oxathiine‐2,1′‐cyclohexan]‐4‐one | —— | C13H14O2S |
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—— | (p-methylthiophenyl)dimesitylborane | —— | C25H29BS |
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—— | 4-cyclopropylthioanisole | —— | C10H12S |
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—— | bis(4-(methylthio)phenyl)dimethylsilane | —— | C16H20S2Si |
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—— | dimethyl(4-(methylthio)phenyl)silanol | —— | C9H14OSSi |
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—— | trans-2-(4-(methylthio)phenyl)cyclohexan-1-ol | —— | C13H18OS |
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—— | 2-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)thio)benzoic acid | —— | C13H7N3O5S |
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—— | 3-(4-(methylthio)phenyl)propiolic acid | —— | C10H8O2S |
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—— | 4-[4-(methylsulfanyl)phenyl]-3-butyn-1-ol | —— | C11H12OS |
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—— | 2-acetoxyimino-benzo[<i>b</i>]thiophen-3-one | —— | C10H7NO3S |
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—— | dimethylsulfoxide-d5 | —— | C2H6OS |
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—— | 2,2'-(propane-2,2-diylbis(sulfanediyl))bis(ethan-1-ol) | —— | C7H16O2S2 |
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—— | 2-(2-(2-(prop-2-ynyloxy)ethyl)disulfanyl)ethanol | 1391914-41-2 | C7H12O2S2 |
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—— | 11-(11-hydroxyundecylsulfanylmethylsulfanyl)undecan-1-ol | —— | C23H48O2S2 |
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—— | (2S)-2-(t-butylthio)-1-propanol | —— | C7H16OS |
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—— | (R)-tert-butyl 1-thioxo-1-(2,2,2-trifluoroethylamino)propan-2-ylcarbamate | —— | C10H17F3N2O2S |
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—— | N-(3-(methylsulfonyl)propyl)prop-2-en-1-amine | —— | C7H15NO2S |
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—— | 1-(4-(methylthio)phenyl)penta-3,4-dien-1-ol | —— | C12H14OS |
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—— | 3-(4-methylsulfanylphenyl)cyclopent-2-en-1-one | —— | C12H12OS |
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—— | (3-fluorobenzyl)(phenyl)sulfane | —— | C13H11FS |
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—— | (2-fluorobenzyl)(phenyl)sulfane | —— | C13H11FS |
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—— | 2-amino-6-<(4-methylphenyl)sulfanyl>purine | —— | C12H11N5S |
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—— | 2-amino-6-(phenylsulfanyl)purine | —— | C11H9N5S |
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—— | 2-amino-7-(2-bromoethyl)-6-<(4-chlorophenyl)sulfanyl>-9H-purine | —— | C13H11BrClN5S |
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—— | tert-butyl 4-hydroxy-2-(methylthio)-5,8-dihydropyrido[3,4-d]pyrimidine-7(6H)-carboxylate | —— | C13H19N3O3S |
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—— | bis-(1-acetoxy-2,2,2-trichloro-ethyl)-sulfide | —— | C8H8Cl6O4S |
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—— | (2-bromo-1,1,2,2-tetrafluoroethyl)(p-tolyl)sulfane | —— | C9H7BrF4S |
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—— | 4-(methylthio)phenyl boroxine | —— | C21H21B3O3S3 |
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—— | ethyl 4-((4-methoxyphenyl)thio)benzoate | —— | C16H16O3S |
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—— | 2-(3-methylbutoxy)-1,3-benzodithiol-4-carboxylic acid methyl ester | —— | C14H18O3S2 |
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