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-<2-(5-methyl-2-thienyl)-1,3-dithial-2-yl>dihydrofuran-2(3H)-one | —— | C13H16O2S3 |
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—— | 3-(2-methyl-1,3-dithian-2-yl)-propanal | —— | C8H14OS2 |
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—— | 2-trimethylsilyloxy-4-(4-(methylthio)phenyl)-3,4-dihydrofuran | —— | C14H22O2SSi |
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—— | di-buta-2,3-dienyl sulfide | —— | C8H10S |
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—— | (2-phenyl-1,3-dithian-2-yl)methanol | —— | C11H14OS2 |
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—— | bis(2-chloro-1-propene-3-ylsulfanyl)methane | —— | C7H10Cl2S2 |
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—— | 2-(2,4-dihydroxyphenylthio)-5-hydroxyphenyl dodecanoate | —— | C24H32O5S |
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—— | 3-amino-5-(3-hydroxypropylthio)-1,2,4-triazole | —— | C5H10N4OS |
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—— | 3-methyl-5-(3-hydroxypropylthio)-1,2,4-triazole | —— | C6H11N3OS |
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—— | 4-amino-2-(3-hydroxypropylthio)pyrimidine | —— | C7H11N3OS |
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—— | 1-(Methanesulfonyl)-3-chloro-propanol | —— | C4H9ClO3S |
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—— | 2-(α,α-difluoromethylthio)pyrimidine | —— | C5H4F2N2S |
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—— | (2-chlorophenyl)(difluoromethyl)sulfane | —— | C7H5ClF2S |
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—— | 2-((difluoromethyl)thio)pyridine | —— | C6H5F2NS |
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—— | 3-difluoromethoxy-4-cyano-5-methylthioisothiazole | —— | C6H4F2N2OS2 |
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—— | (4-(difluoromethyl)phenyl)(ethyl)sulfane | —— | C9H10F2S |
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—— | difluoromethyl methyl sulfone | —— | C2H4F2O2S |
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—— | (Z)-1-phenylthio-2-butyltelluro-1-hexene | —— | C16H24STe |
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—— | 8-(4-chloro-phenylsulfanylmethyl)-8-methyl-6,7,10-trioxa-spiro-[4.5]decane | —— | C15H19ClO3S |
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—— | 2-{2-[5-((5-(pyridin-3-yl)-1,3,4-thiadiazol-2-ylamino)methyl)-1,3,4-oxadiazol-2-ylthio]ethoxy}ethanol | —— | C14H16N6O3S2 |
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—— | bis[2-(2-hydroxyethoxy)ethylthio]maleonitrile | —— | C12H18N2O4S2 |
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—— | acrylaldehyde diphenyldithioacetal | —— | C15H14S2 |
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—— | 2-(2-((5-methyl-1,3,4-thiadiazol-2-yl)thio)ethoxy)ethan-1-ol | —— | C7H12N2O2S2 |
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—— | 4-[(p-chlorophenyl)-2-trichloromethylsulfanyl]triazole | —— | C10H5Cl4NS2 |
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—— | 8-(ethylthio)-6-methyl-7-azabicyclo<4.2.0>octa-3,7-diene | —— | C10H15NS |
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—— | 3-hydroxy-2-phenylthiobenzo[b]thiophene | —— | C14H10OS2 |
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—— | 1,2-hexene oxide | —— | C13H20OS |
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—— | 1,2-hexene oxide | —— | C12H17ClOS |
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—— | 1-cyano-1-thiophenyl-2,2-bis(thio-3'-chloroallyl)ethylene | —— | C15H9Cl2NS3 |
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—— | 2-[2-(1-adamantyl)-1,3,4-oxadiazol-5-ylthio]acetic acid | —— | C14H18N2O3S |
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—— | bis((E)-1-chloro-1-propen-3-yl) disulfide | —— | C6H8Cl2S2 |
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—— | [1,2,4]thiadiazole-3,5-diyldimercapto-di-acetic acid | —— | C6H6N2O4S3 |
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—— | nitro-4-sulfinylbenzoic acid | —— | C7H5NO5S |
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—— | p-tolyl(4-(trifluoromethyl)phenyl)sulfane | —— | C14H11F3S |
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—— | N-methoxy-N-methyl-2-(p-tolylthio)acetamide | —— | C11H15NO2S |
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—— | 3-formyl-6-methoxyphenyl 4-tolyl sulfide | —— | C15H14O2S |
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—— | 6-chloro-3-chloromethyl-7-methyl-2,3-dihydro-1,4,2-benzodithiazine 1,1-dioxide | —— | C9H9Cl2NO2S2 |
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—— | 3,4-dimethoxyphenyl 4-tolyl sulfide | —— | C15H16O2S |
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—— | 2-methyl-3-oxo-2-phenyl-5,7-bis(p-tolylsulphanyl)indoline | —— | C29H25NOS2 |
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—— | dihexyl thiourea | —— | C13H28N2S |
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—— | 1,2-bis-[6-phenyl-1,2,4-triazolo[3,4-b][1,3,4]thiadiazin-3-yl]ethan-1-ol | —— | C22H18N8OS2 |
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—— | <i>N</i>,<i>N</i>'-bis-(2,2-diethoxy-ethyl)-thiourea | —— | C13H28N2O4S |
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—— | 3-cyanobicyclo[1.1.1]pentan-1-ylthiourea | —— | C7H9N3S |
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—— | 5-acetyl-6-methylsulfanyl-2-phenylpyrimidine-4(3H)-thione | —— | C13H12N2OS2 |
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—— | 2-(methylthio)imidazo[2,1-b][1,3,4]thiadiazole-6-carbonyl chloride | —— | C6H4ClN3OS2 |
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—— | 2-(methylthio)imidazo[2,1-b][1,3,4]thiadiazole-6-carboxylic acid | —— | C6H5N3O2S2 |
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—— | 3-(2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)-7H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazine | —— | C10H10N6S |
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—— | 11-phenyl-11H-dibenzo[b,f][1,4]dithiepin | —— | C19H14S2 |
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—— | 2,2-dimethyl-1-[2-(2-sulfanylphenylsulfanyl)phenyl]-1-propanol | —— | C17H20OS2 |
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—— | 2-(4-aminophenylsulfinyl)diphenyl sulfide | —— | C18H15NOS2 |
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