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 |
---|---|---|---|---|
—— | 4-methyl-2-phenylsulfanylcyclohexanone | —— | C13H16OS |
|
—— | 7-cyano-5-(pyridin-3-yl)-2,3-dihydropyrrolo[2,1-b]thiazole hydrochloride | —— | C12H9N3S*ClH |
|
—— | but-3-enethioic acid N-butyl-N-methylamide | —— | C9H17NS |
|
—— | 3-[4-((N',N'-dimethylaminocarbonyl)amino)phenylthio]bromobenzene | —— | C15H15BrN2OS |
|
—— | 9-tert-butyl-3-(4-chlorophenylsulfanylmethyl)-3-methyl-1,2,5-trioxaspiro[5.5]undecane | —— | C20H29ClO3S |
|
—— | 3-amino-3-(butylmethylamino)-2-cyanopropenethioamide | —— | C9H16N4S |
|
—— | S-methyl N-butyl-N-methylthiocarbamate | —— | C7H15NOS |
|
—— | 2-(tert-butyl)-5-((2-chloropyridin-4-yl)thio)-1-((tetrahydro-2H-pyran-4-yl)methyl)-1H-benzo[d]imidazole | —— | C22H26ClN3OS |
|
—— | phenyl(1,1,2,2-tetrafluorotetradecyl)sulfane | —— | C20H30F4S |
|
—— | t-butyl dodecyl sulfone | —— | C16H34O2S |
|
—— | 3-[2-(dimethylamino)-4-hydroxyphenylthio]pentane-2,4-dione | —— | C13H17NO3S |
|
—— | 4-methyl-2-(p-tolylthio)aniline | —— | C14H15NS |
|
—— | 3-(4-bromophenyl)-5-(p-tolylthio)-1,2,4-thiadiazole | —— | C15H11BrN2S2 |
|
—— | 2-methyl-1-[(4-methylphenyl)thio]-2-propanamine | —— | C11H17NS |
|
—— | (2-methylthiophenyl)(p-tolyl)sulfane | —— | C14H14S2 |
|
—— | 1-(p-tolylthio)naphthalen-2-amine | —— | C17H15NS |
|
—— | 3-phenyl-5-(p-tolylthio)-1,2,4-thiadiazole | —— | C15H12N2S2 |
|
—— | methyl 4-(5-(p-tolylthio)-1,2,4-thiadiazol-3-yl)benzoate | —— | C17H14N2O2S2 |
|
—— | 3-(4-nitrophenyl)-5-(p-tolylthio)-1,2,4-thiadiazole | —— | C15H11N3O2S2 |
|
—— | (4-methylphenyl)(perfluorobutyl)sulfane | —— | C11H7F9S |
|
—— | 4-(p-methylphenylthio)dihydrolevoglucosenone | —— | C13H14O3S |
|
—— | 2-methyl-1-[(4-methylphenyl)sulfanyl]propan-2-ol | —— | C11H16OS |
|
—— | 1-(thiophen-3-yl)-2-(p-tolylthio)ethanone | —— | C13H12OS2 |
|
—— | 3-methyl-4-(p-tolylthio)aniline | —— | C14H15NS |
|
—— | 2-chloro-4-(p-tolylthio)quinazoline | —— | C15H11ClN2S |
|
—— | 2-methoxy-4-(p-tolylthio)aniline | —— | C14H15NOS |
|
—— | 4-hydroxy-3-[(4-methylphenyl)sulfanyl]pent-3-en-2-one | —— | C12H14O2S |
|
—— | (4-(tert-butyl)phenyl)(p-tolyl)sulfane | —— | C17H20S |
|
—— | 5-(p-tolylthio)pyrimidine | —— | C11H10N2S |
|
—— | (Z)-(1,1,1,4,4,4-hexafluorobut-2-en-2-yl)(p-tolyl)sulfane | —— | C11H8F6S |
|
—— | 3-bromo-4-(p-tolylthio)pyridine | —— | C12H10BrNS |
|
—— | 5-(4-tolyl)thio-6-chlorouracil | —— | C11H9ClN2O2S |
|
—— | 1-(2-methyl-5-(phenyl(p-tolylthio)methyl)furan-3-yl)ethan-1-one | —— | C21H20O2S |
|
—— | 6-methyl-5-(p-tolylthio)pyrimidine-2,4(1H,3H)-dione | —— | C12H12N2O2S |
|
—— | 2-(p-tolylthio)benzonitrile | —— | C14H11NS |
|
—— | 2,6-dimethyl-4-(p-tolylthio)aniline | —— | C15H17NS |
|
—— | (S)-2-[bis(4-methylphenylthio)methyl]pyrrolidine | —— | C19H23NS2 |
|
—— | (4-chlorophenethyl)(p-tolyl)sulfane | —— | C15H15ClS |
|
—— | 1-(4-methylphenylthio)butan-2-ol | —— | C11H16OS |
|
—— | (3,5-dimethyl phenyl) (p-tolyl)sulfane | —— | C15H16S |
|
—— | 2-methyl-3-(p-tolylthio)-1H-indole | —— | C16H15NS |
|
—— | 2,8-dimethyl-6H,12H-dibenzo<b,f><1,5>dithiocin | —— | C16H16S2 |
|
—— | 3-[(4-methylphenyl)thio]-1-propanethiol | —— | C10H14S2 |
|
—— | 5,6-dihydrothiazolo[3.2-d]tetrazole | —— | C3H4N4S |
|
—— | 3-ethyl-3-isothiocyanatooctane | —— | C11H21NS |
|
—— | 1-bromo-4-methylthiobutane | —— | C5H11BrS |
|
—— | 2-(4-(methylthio)-1H-pyrazol-1-yl)acetonitrile | —— | C6H7N3S |
|
—— | 3-ethyl-3-isothiocyanatononane | —— | C12H23NS |
|
—— | 3-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-5-[(4-methylphenyl)sulfanyl]-1,2,4-thiadiazole | —— | C14H16N2O2S2 |
|
—— | 3-phenethyl-5-(p-tolylthio)-1,2,4-thiadiazole | —— | C17H16N2S2 |
|