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 |
---|---|---|---|---|
—— | (1R)-1-[3-chloro-4-(1,3-thiazol-2-ylsulfanyl)phenyl]-N-methylethanamine | —— | C12H13ClN2S2 |
|
—— | (1R)-1-[3-chloro-4-[(4-methyl-1,2,4-triazol-3-yl)sulfanyl]phenyl]-N-methylethanamine | —— | C12H15ClN4S |
|
—— | (1R)-1-(4-tert-butylsulfanyl-3-chlorophenyl)-N-ethylethanamine | —— | C14H22ClNS |
|
—— | (1R)-1-[3-chloro-4-[(4-methyl-1,3-thiazol-2-yl)sulfanyl]phenyl]-N-methylethanamine | —— | C13H15ClN2S2 |
|
—— | (1R)-1-[3-bromo-4-(1H-1,2,4-triazol-5-ylsulfanyl)phenyl]-N-ethylethanamine | —— | C12H15BrN4S |
|
—— | (1S)-1-[3-bromo-4-(2-methoxyethylsulfanyl)phenyl]-N-ethylethanamine | —— | C13H20BrNOS |
|
—— | (1R)-1-[3-chloro-4-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]phenyl]-N-methylethanamine | —— | C12H14ClN3S2 |
|
—— | (2R)-2-(3-bromo-4-fluorophenyl)-2-thiophen-2-ylsulfanylpropanoic acid | —— | C13H10BrFO2S2 |
|
—— | (2S)-2-(3-bromo-4-fluorophenyl)-2-thiophen-2-ylsulfanylpropanoic acid | —— | C13H10BrFO2S2 |
|
—— | (2Z)-2-[(2-aminoanilino)methylidene]-1-benzothiophen-3-one | —— | C15H12N2OS |
|
—— | (2E)-2-[1-(3-methylanilino)ethylidene]-1-benzothiophen-3-one | —— | C17H15NOS |
|
—— | (2E)-2-[(3-methylanilino)methylidene]-1-benzothiophen-3-one | —— | C16H13NOS |
|
—— | (2E)-2-[1-(2,4-dimethylanilino)ethylidene]-1-benzothiophen-3-one | —— | C18H17NOS |
|
—— | (2Z)-2-[1-(3-chloroanilino)ethylidene]-1-benzothiophen-3-one | —— | C16H12ClNOS |
|
—— | (2E)-2-[(3,4-dimethylanilino)methylidene]-1-benzothiophen-3-one | —— | C17H15NOS |
|
—— | (2Z)-2-[1-(2-hydroxyanilino)ethylidene]-1-benzothiophen-3-one | —— | C16H13NO2S |
|
—— | 2-[1-p-Tolylamino-eth-(E)-ylidene]-benzo[b]thiophen-3-one | 126318-43-2 | C17H15NOS |
|
—— | (2R)-2-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]butanamide | —— | C7H11N3OS2 |
|
—— | (NZ)-N-(4-methoxy-5,7,8,9-tetrahydropyrimido[4,5-b][1,4]benzothiazin-6-ylidene)hydroxylamine | —— | C11H12N4O2S |
|
—— | (2S)-2-[5-(trifluoromethyl)pyridin-2-yl]sulfanylbutanamide | —— | C10H11F3N2OS |
|
—— | [(Z)-(3-ethylsulfanylthiophen-2-yl)methylideneamino]urea | —— | C8H11N3OS2 |
|
—— | (2R)-2-[(4-methyl-1,3-thiazol-2-yl)sulfanyl]butanamide | —— | C8H12N2OS2 |
|
—— | (2S)-2-[(4-methyl-1,3-thiazol-2-yl)sulfanyl]butanamide | —— | C8H12N2OS2 |
|
—— | (2R)-2-[5-(trifluoromethyl)pyridin-2-yl]sulfanylbutanamide | —— | C10H11F3N2OS |
|
—— | (2R)-2-(2,5-dimethylphenyl)sulfanylbutanamide | —— | C12H17NOS |
|
—— | (2R)-2-(2-bromophenyl)sulfanylbutanamide | —— | C10H12BrNOS |
|
—— | (2R)-2-(4,6-diaminopyrimidin-2-yl)sulfanylbutanamide | —— | C8H13N5OS |
|
—— | (2S)-2-(4-amino-2,6-difluorophenyl)sulfanylbutanamide | —— | C10H12F2N2OS |
|
—— | (2S)-2-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]butanamide | —— | C7H11N3OS2 |
|
—— | [(Z)-[2-(4,6-dimethylpyrimidin-2-yl)sulfanyl-1-phenylethylidene]amino]urea | —— | C15H17N5OS |
|
—— | (2R)-2-[(5-amino-4-methyl-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C7H13N5OS |
|
—— | (2R)-2-(5-aminopyridin-2-yl)sulfanylbutanamide | —— | C9H13N3OS |
|
—— | N-[(Z)-benzylideneamino]-2-(6-methyl-2-methylsulfanylpyrimidin-4-yl)sulfanylacetamide | —— | C15H16N4OS2 |
|
—— | (2S)-2-(2-amino-4-fluorophenyl)sulfanylbutanamide | —— | C10H13FN2OS |
|
—— | (2S)-2-[(5-oxo-4-propyl-1H-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C9H16N4O2S |
|
—— | (2S)-2-[(5-amino-4-methyl-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C7H13N5OS |
|
—— | (2S)-2-(2-aminophenyl)sulfanylbutanamide | —— | C10H14N2OS |
|
—— | (2S)-2-(2-bromophenyl)sulfanylbutanamide | —— | C10H12BrNOS |
|
—— | (2S)-2-(2,5-dimethylphenyl)sulfanylbutanamide | —— | C12H17NOS |
|
—— | (2S)-2-(3-aminopyridin-2-yl)sulfanylbutanamide | —— | C9H13N3OS |
|
—— | (2R)-2-(4-amino-2-methylphenyl)sulfanylbutanamide | —— | C11H16N2OS |
|
—— | (2R)-2-(4-amino-2,6-difluorophenyl)sulfanylbutanamide | —— | C10H12F2N2OS |
|
—— | (2R)-2-[(6-amino-4-oxo-1H-pyrimidin-2-yl)sulfanyl]butanamide | —— | C8H12N4O2S |
|
—— | (2R)-2-(4-aminophenyl)sulfanylbutanamide | —— | C10H14N2OS |
|
—— | (2R)-2-[(5-oxo-4-propyl-1H-1,2,4-triazol-3-yl)sulfanyl]butanamide | —— | C9H16N4O2S |
|
—— | (2S)-2-(4,6-diaminopyrimidin-2-yl)sulfanylbutanamide | —— | C8H13N5OS |
|
—— | (2Z)-2-[(3-hydroxyanilino)methylidene]-1-benzothiophen-3-one | —— | C15H11NO2S |
|
—— | (2R)-2-(4-amino-2-fluorophenyl)sulfanylbutanamide | —— | C10H13FN2OS |
|
—— | (2R)-2-(2-amino-6-chlorophenyl)sulfanylbutanamide | —— | C10H13ClN2OS |
|
—— | (2S)-2-(4-aminophenyl)sulfanylbutanamide | —— | C10H14N2OS |
|