摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

有机硫化合物

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:

  • 二硫化物:含-S-S-键的化合物。
  • 硫醚(Thiols):含有-R-S-H或-R-S-R 基团的化合物。
  • 磺酸酯(Sulfonates)与磺酸盐(Sulfonates):带有-SO3H基团的化合物,广泛应用于合成和制药领域。
  • 噻吩及其衍生物:具有环状结构的有机硫化物。
2. 生物学活性

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:

  • 某些硫醚类药物被用于抗真菌、抗菌以及抗癌治疗。
  • 硫代葡萄糖苷(Glycosinolate)是十字花科植物中的一种天然存在物质,具有生物活性。
3. 合成方法

有机硫化合物可通过多种途径合成:

  • 亲核取代反应:使用含硫试剂与卤化物进行反应。
  • 自由基加成法:采用氧化剂引发自由基形成,通过烯烃与H2S、R-S-H等反应制备。
  • 金属催化转化:利用钯、铜等催化剂促进特定硫化过程。
4. 应用领域

有机硫化合物的应用广泛:

  • 医药领域:用于开发抗菌剂、抗病毒药物及抗癌药物等。
  • 农学研究:某些有机硫化合物作为生物农药的有效成分,能够抑制病害的发生。
  • 材料科学与技术:在导电聚合物和塑料添加剂中有重要应用。
5. 环境与安全性

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
—— platinum;sulfur dioxide;tri(propan-2-yl)phosphane 184361-39-5 C18H42O2P2PtS
platinum;sulfur dioxide;tri(propan-2-yl)phosphane
—— (3RS,5S,3'EZ)-3-(4'-iodo-3'-butenyl)-5-methyl-3-(phenylsulfanyl)tetrahydrofuran-2-one 210160-15-9 C15H17IO2S
(3RS,5S,3'EZ)-3-(4'-iodo-3'-butenyl)-5-methyl-3-(phenylsulfanyl)tetrahydrofuran-2-one
—— 2-methyl-2-(trifluoromethyltrisulfanyl)propane 145372-19-6 C5H9F3S3
2-methyl-2-(trifluoromethyltrisulfanyl)propane
—— Dichloro(methylsulfanylmethane)selenium(II) 1422977-82-9 C2H6Cl2SSe
Dichloro(methylsulfanylmethane)selenium(II)
—— cis-[PtCl<sub>2</sub>((PhSCH<sub>2</sub>)<sub>2</sub>Si<sub>2</sub>Me<sub>4</sub>)] 882054-16-2 C18H26Cl2PtS2Si2
cis-[PtCl<sub>2</sub>((PhSCH<sub>2</sub>)<sub>2</sub>Si<sub>2</sub>Me<sub>4</sub>)]
—— diazo-methane, diazomethane sodium 67880-28-8 CHN2Na
diazo-methane, diazomethane sodium
—— 1-thiocyanato-but-1-yne 57562-94-4 C5H5NS
1-thiocyanato-but-1-yne
—— bis(disulfaneyl)selane 163893-19-4 H2S4Se
bis(disulfaneyl)selane
—— dibromobis(diethyl sulfide) palladium (II) 14784-46-4 C8H20Br2PdS2
dibromobis(diethyl sulfide) palladium (II)
—— cyanothioacetamide 503621-72-5 C3H4N2S
cyanothioacetamide
—— 6-ethylsulfanyl-hexa-1,3-dien-5-yne 13984-36-6 C8H10S
6-ethylsulfanyl-hexa-1,3-dien-5-yne
—— 1,9-diphenyl-1,5,9-trithianonane 77400-55-6 C18H22S3
1,9-diphenyl-1,5,9-trithianonane
—— (4R,5S,6R)-4-((S)-1-{2-[(2R,3S,4R)-2,4-bis(tert-butyldimethylsilanyloxy)-3,5-dimethylhexyl]-[1,3]dithian-2-yl}-ethyl)-6-((S)-1-methoxy-prop-2-ynyl)-2,2,5-trimethyl-[1,3]dioxane 381246-87-3 C37H72O5S2Si2
(4R,5S,6R)-4-((S)-1-{2-[(2R,3S,4R)-2,4-bis(tert-butyldimethylsilanyloxy)-3,5-dimethylhexyl]-[1,3]dithian-2-yl}-ethyl)-6-((S)-1-methoxy-prop-2-ynyl)-2,2,5-trimethyl-[1,3]dioxane
—— 2-bromo-5-(ethylthio)pyridine 1346539-39-6 C7H8BrNS
2-bromo-5-(ethylthio)pyridine
—— 89829-40-3 C4H10S*I5Ta
—— [PtI(1,9-diphenyl-1,5,9-trithianonane)][BF4] 181699-25-2 BF4*C18H22IPtS3
[PtI(1,9-diphenyl-1,5,9-trithianonane)][BF4]
—— (1R)-1-[(4R,5S,6R)-6-((S)-1-{2-[(2R,3S,4R)-2,4-bis(tert-butyldimethylsilanyloxy)-3,5-dimethylhexyl]-[1,3]dithian-2-yl}-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-prop-2-yn-1-ol 381246-85-1 C36H70O5S2Si2
(1R)-1-[(4R,5S,6R)-6-((S)-1-{2-[(2R,3S,4R)-2,4-bis(tert-butyldimethylsilanyloxy)-3,5-dimethylhexyl]-[1,3]dithian-2-yl}-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-prop-2-yn-1-ol
—— 1-[(4R,5S,6R)-6-((S)-1-{2-[(2R,3S,4R)-2,4-Bis-(tert-butyl-dimethyl-silanyloxy)-3,5-dimethyl-hexyl]-[1,3]dithian-2-yl}-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-propynone 381246-71-5 C36H68O5S2Si2
1-[(4R,5S,6R)-6-((S)-1-{2-[(2R,3S,4R)-2,4-Bis-(tert-butyl-dimethyl-silanyloxy)-3,5-dimethyl-hexyl]-[1,3]dithian-2-yl}-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-propynone
—— 33726-43-1 C4H10S*Cl5Nb
—— trans-{Ir(C4H10S)3Cl3}*CHCl3 149165-70-8 CHCl3*C12H30Cl3IrS3
trans-{Ir(C4H10S)3Cl3}*CHCl3
—— methyl (1S,4R,4aS,5R,8S,8aR)-1,3,4,5,8,8a-hexahydro-5-(phenylthio)-8-[2-((2R,4R,6S)-tetrahydro-4,6-dimethoxy-2H-pyran-2-yl)-ethyl]-1,4-epoxynaphthalene-4a(2H)-carboxylate 84751-40-6 C27H36O6S
methyl (1S,4R,4aS,5R,8S,8aR)-1,3,4,5,8,8a-hexahydro-5-(phenylthio)-8-[2-((2R,4R,6S)-tetrahydro-4,6-dimethoxy-2H-pyran-2-yl)-ethyl]-1,4-epoxynaphthalene-4a(2H)-carboxylate
—— nonafluoro-tert-butyl(pentafluorophenyl)sulfane 60214-22-4 C10F14S
nonafluoro-tert-butyl(pentafluorophenyl)sulfane
—— dithiooxalodiimidic acid dipropyl ester 127952-89-0 C8H16N2S2
dithiooxalodiimidic acid dipropyl ester
—— monoselenotetrathionic acid 61559-39-5 H2O6S3Se
monoselenotetrathionic acid
—— (dimethyldithiocarbamato)hydrido(triethylphosphine)platinum(II) 124176-57-4 C9H22NPPtS2
(dimethyldithiocarbamato)hydrido(triethylphosphine)platinum(II)
—— (chloro)(dimethyl sulfoxide)(1,2-diaminoethane)platinium(II) chloride 91513-56-3 C4H14ClN2OPtS*Cl
(chloro)(dimethyl sulfoxide)(1,2-diaminoethane)platinium(II) chloride
—— iodo(triphenylphosphane)(4-amino-3-methyl-1,2,4-triazol-5-thione)palladium chloride 1258555-45-1 C21H21IN4PPdS*Cl
iodo(triphenylphosphane)(4-amino-3-methyl-1,2,4-triazol-5-thione)palladium chloride
—— (TMEDA)Zn(S6) 162557-46-2 C6H16N2S6Zn
(TMEDA)Zn(S6)
—— Mercury, (benzenethiolato)methyl- 17019-36-2 C7H8HgS
Mercury, (benzenethiolato)methyl-
—— 7-bromo-3-[(4-methylphenyl)imino][1]benzothiophen-2(3H)-one 1283157-83-4 C15H10BrNOS
7-bromo-3-[(4-methylphenyl)imino][1]benzothiophen-2(3H)-one
—— Cyanoguanyl-imido-dithiokohlensaeuredimethylester 15048-19-8 C5H8N4S2
Cyanoguanyl-imido-dithiokohlensaeuredimethylester
—— 4-bromo-3-(phenylthio)-2-sulfolene 114397-08-9 C10H9BrO2S2
4-bromo-3-(phenylthio)-2-sulfolene
—— (3RS,5S)-3-(2'-formylethyl)-5-methyl-3-(phenylsulfanyl)tetrahydrofuran-2-one 210160-17-1 C14H16O3S
(3RS,5S)-3-(2'-formylethyl)-5-methyl-3-(phenylsulfanyl)tetrahydrofuran-2-one
—— 381247-22-9 C34H68O5S2Si2
—— diethyl-propyl sulfonium ; iodide 52238-43-4 C7H17S*I
diethyl-propyl sulfonium ; iodide
—— 176241-87-5 C6H16S2
—— 108616-88-2 C15H23N5NiO4S2
—— 5-fluoro-6-phenylthio-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)-2'-deoxyuridine 98495-63-7 C27H41FN2O6SSi2
5-fluoro-6-phenylthio-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)-2'-deoxyuridine
—— ethanethiol, tetraethyl tetrathioorthostannate 16528-52-2 4C2H5S*Sn
ethanethiol, tetraethyl tetrathioorthostannate
—— 1403980-23-3 C7H9I
—— 1,1,2,2-tetraethyl-1λ4,2λ4-disulfene radical cation 51137-16-7 C8H20S2
1,1,2,2-tetraethyl-1λ4,2λ4-disulfene radical cation
—— 107534-92-9 Br*C4H10S
—— (2-pentafluoroethyl-4,5-dimethylphenyl)ethylsulfide 1400258-82-3 C12H13F5S
(2-pentafluoroethyl-4,5-dimethylphenyl)ethylsulfide
—— bis(N,N-diethyldithiocarbamato)tin(II) 17188-90-8 2C5H10NS2*Sn
bis(N,N-diethyldithiocarbamato)tin(II)
—— trans-halogeno-(RuBr2(Me2SO)(Et2S)3) 99028-99-6 C14H36Br2ORuS4
trans-halogeno-(RuBr2(Me2SO)(Et2S)3)
—— 73375-82-3 C10H20As2I6N2NiS4
—— 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthylthio)benzoyl chloride 173157-31-8 C22H25ClOS
4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthylthio)benzoyl chloride
—— [Os(CS)(PCy3)2I2] 952649-10-4 C37H66I2OsP2S
[Os(CS)(PCy3)2I2]
—— tetraethyloxoosmium(VI) 130149-63-2 C8H20OOs
tetraethyloxoosmium(VI)
—— pinacol 2-phenyl-1-(phenylthio)ethane-1-boronate 66080-30-6 C20H25BO2S
pinacol 2-phenyl-1-(phenylthio)ethane-1-boronate