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 |
---|---|---|---|---|
—— | (2R)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-(3,5-dimethylpyrazol-1-yl)propanamide | —— | C16H16ClN5OS2 |
|
—— | (1S,2S)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-(3-fluorophenyl)cyclopropane-1-carboxamide | —— | C18H13ClFN3OS2 |
|
—— | (1R,2S)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-(3-fluorophenyl)cyclopropane-1-carboxamide | —— | C18H13ClFN3OS2 |
|
—— | (2S)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-phenylmethoxypropanamide | —— | C18H16ClN3O2S2 |
|
—— | (2R)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-cyclopentyloxy-2-phenylacetamide | —— | C21H20ClN3O2S2 |
|
—— | (2R)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-2-phenylmethoxypropanamide | —— | C18H16ClN3O2S2 |
|
—— | 3-(4-chlorophenyl)sulfanyl-N-(4-phenylbutan-2-yl)propanamide | —— | C19H22ClNOS |
|
—— | (2S)-3-(4-fluorophenyl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-2-(5-methyltetrazol-1-yl)propanamide | —— | C24H22FN5O2S |
|
—— | (3R)-1-(2,2-dimethylpropanoyl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]piperidine-3-carboxamide | —— | C24H30N2O3S |
|
—— | (2S)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-2,3-dihydro-1-benzofuran-2-carboxamide | —— | C22H19NO3S |
|
—— | (3S)-1-(cyclopropanecarbonyl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]piperidine-3-carboxamide | —— | C23H26N2O3S |
|
—— | (3S)-N-[3-chloro-4-(1,3,4-thiadiazol-2-ylsulfanyl)phenyl]-1-[(2S)-2-methylbutanoyl]piperidine-3-carboxamide | —— | C19H23ClN4O2S2 |
|
—— | (2R)-3-(3-fluorophenyl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-2-(5-methyltetrazol-1-yl)propanamide | —— | C24H22FN5O2S |
|
—— | (2R)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-2,3-dihydro-1-benzofuran-2-carboxamide | —— | C22H19NO3S |
|
—— | (2R)-3-(4-fluorophenyl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-2-(5-methyltetrazol-1-yl)propanamide | —— | C24H22FN5O2S |
|
—— | (3R)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-1-[(2S)-2-methylbutanoyl]piperidine-3-carboxamide | —— | C24H30N2O3S |
|
—— | (3S)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-1-[(2S)-2-methylbutanoyl]piperidine-3-carboxamide | —— | C24H30N2O3S |
|
—— | (3S)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-1-[(2R)-2-methylbutanoyl]piperidine-3-carboxamide | —— | C24H30N2O3S |
|
—— | (3R)-N-[4-(4-methoxyphenyl)sulfanylphenyl]-1-[(2R)-2-methylbutanoyl]piperidine-3-carboxamide | —— | C24H30N2O3S |
|
—— | (2S)-2-(3,5-dimethylpyrazol-1-yl)-N-[4-(4-methoxyphenyl)sulfanylphenyl]propanamide | —— | C21H23N3O2S |
|
—— | 6-Acetyl-2-(3-chlorophenyl)-5-methyl-4-(4-nitrophenyl)sulfanylpyridazin-3-one | —— | C19H14ClN3O4S |
|
—— | (3Z,6Z)-3-benzylidene-6-[[4-[2-(dimethylamino)ethylsulfanyl]phenyl]methylidene]piperazine-2,5-dione;hydrochloride | —— | C22H24ClN3O2S |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(2S)-2-phenylpropyl]propanamide | —— | C18H20BrNOS |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(2R)-2-phenylpropyl]propanamide | —— | C18H20BrNOS |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(3R)-1,1-dioxothiolan-3-yl]-N-ethylpropanamide | —— | C15H20BrNO3S2 |
|
—— | 2-(3-bromophenyl)sulfanyl-1-[4-[(3R)-1,1-dioxothiolan-3-yl]piperazin-1-yl]ethanone | —— | C16H21BrN2O3S2 |
|
—— | (2S)-1-(4-acetyl-3,5-dimethyl-1H-pyrrol-2-yl)-2-(3-bromophenyl)sulfanylpropan-1-one | —— | C17H18BrNO2S |
|
—— | 2-(3-bromophenyl)sulfanyl-1-[1-[(3S)-1,1-dioxothiolan-3-yl]-2,5-dimethylpyrrol-3-yl]ethanone | —— | C18H20BrNO3S2 |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(3R)-1,1-dioxothiolan-3-yl]-N-methylpropanamide | —— | C14H18BrNO3S2 |
|
—— | 2-(3-bromophenyl)sulfanyl-N-cyclohexyl-N-[(3R)-1,1-dioxothiolan-3-yl]acetamide | —— | C18H24BrNO3S2 |
|
—— | 2-(3-bromophenyl)sulfanyl-N-cyclohexyl-N-[(3S)-1,1-dioxothiolan-3-yl]acetamide | —— | C18H24BrNO3S2 |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(3-fluorophenyl)methyl]-N-methylpropanamide | —— | C17H17BrFNOS |
|
—— | 2-(3-bromophenyl)sulfanyl-N-[(3S)-1,1-dioxothiolan-3-yl]-N-(thiophen-2-ylmethyl)acetamide | —— | C17H18BrNO3S3 |
|
—— | (2S)-2-(3-bromophenyl)sulfanyl-N-[(3S)-1,1-dioxothiolan-3-yl]-N-methylpropanamide | —— | C14H18BrNO3S2 |
|
—— | (2S)-2-(3-bromophenyl)sulfanyl-N-[(3S)-1,1-dioxothiolan-3-yl]-N-ethylpropanamide | —— | C15H20BrNO3S2 |
|
—— | 2-[(1R)-1-(3-bromophenyl)sulfanylethyl]-5-(4-methylphenyl)-1,3,4-oxadiazole | —— | C17H15BrN2OS |
|
—— | 2-(3-bromophenyl)sulfanyl-1-[4-[(3S)-1,1-dioxothiolan-3-yl]piperazin-1-yl]ethanone | —— | C16H21BrN2O3S2 |
|
—— | 2-(3-bromophenyl)sulfanyl-N-[(1R)-1-(4-fluorophenyl)ethyl]-N-methylacetamide | —— | C17H17BrFNOS |
|
—— | 2-(3-bromophenyl)sulfanyl-N-[(1S)-1-(4-fluorophenyl)ethyl]-N-methylacetamide | —— | C17H17BrFNOS |
|
—— | 2-(3-bromophenyl)sulfanyl-N-[[(2S)-4-(2-methylpropyl)morpholin-2-yl]methyl]acetamide | —— | C17H25BrN2O2S |
|
—— | 2-[(1S)-1-(3-bromophenyl)sulfanylethyl]-5-(4-methylphenyl)-1,3,4-oxadiazole | —— | C17H15BrN2OS |
|
—— | 2-(3-bromophenyl)sulfanyl-N-cyclopentyl-N-[(3S)-1,1-dioxothiolan-3-yl]acetamide | —— | C17H22BrNO3S2 |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(3S)-1,1-dioxothiolan-3-yl]-N-ethylpropanamide | —— | C15H20BrNO3S2 |
|
—— | (2R)-4-(3-bromophenyl)sulfanyl-3-oxo-2-(4-phenyl-1,3-thiazol-2-yl)butanenitrile | —— | C19H13BrN2OS2 |
|
—— | 1-[(3S)-3,5-bis(furan-2-yl)-3,4-dihydropyrazol-2-yl]-2-(3-bromophenyl)sulfanylethanone | —— | C19H15BrN2O3S |
|
—— | 2-[(1S)-1-(3-bromophenyl)sulfanylethyl]-5-thiophen-2-yl-1,3,4-oxadiazole | —— | C14H11BrN2OS2 |
|
—— | (2S)-2-(3-bromophenyl)sulfanyl-N-[(3-fluorophenyl)methyl]-N-methylpropanamide | —— | C17H17BrFNOS |
|
—— | 2-[(1R)-1-(3-bromophenyl)sulfanylethyl]-5-thiophen-2-yl-1,3,4-oxadiazole | —— | C14H11BrN2OS2 |
|
—— | (2S)-4-(3-bromophenyl)sulfanyl-3-oxo-2-(4-phenyl-1,3-thiazol-2-yl)butanenitrile | —— | C19H13BrN2OS2 |
|
—— | (2R)-2-(3-bromophenyl)sulfanyl-N-[(3S)-1,1-dioxothiolan-3-yl]-N-methylpropanamide | —— | C14H18BrNO3S2 |
|