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2,2-dimethylbenzo[d][1,3]oxathiole | 7740-07-0

中文名称
——
中文别名
——
英文名称
2,2-dimethylbenzo[d][1,3]oxathiole
英文别名
2,2-dimethyl-1,3-benzoxathiole;2,2-Dimethyl-benz[1,3]oxathiol;2,2-Dimethyl-1,3-benzoxathiol
2,2-dimethylbenzo[d][1,3]oxathiole化学式
CAS
7740-07-0
化学式
C9H10OS
mdl
——
分子量
166.244
InChiKey
KREIDUINHPOIDI-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    60 °C(Press: 1.5 Torr)
  • 密度:
    1.127±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:e6240158c7a0ed777ad08c0f19ccccc2
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,2-dimethylbenzo[d][1,3]oxathiolelithium diethylamide 作用下, 以 六甲基磷酰三胺 为溶剂, 反应 12.0h, 以57%的产率得到2-羟基苯硫酚
    参考文献:
    名称:
    Melis, Stefana; Piras, Pier Paolo; Plumitallo, Antonio, Journal of Heterocyclic Chemistry, 1983, vol. 20, p. 1413 - 1414
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Selective arylthiolane deprotection by singlet oxygen: a promising tool for sensors and prodrugs
    摘要:
    一种常规的硫代烷基保护基与单线态氧迅速且选择性地反应,以揭示酮产物,产率从良好(芳基1,3-二硫杂环)到优秀(芳基1,3-氧硫杂环)。芳基硫代杂环对生物相关的活性氧物种稳定,并可用作激活荧光传感器或小分子前药的光激活门控机制。
    DOI:
    10.1039/c4cc09040c
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文献信息

  • [EN] AMINE DERIVATIVES AS POTASSIUM CHANNEL BLOCKERS<br/>[FR] DÉRIVÉS D'AMINE AGISSANT COMME BLOQUEURS DU CANAL POTASSIUM
    申请人:BIONOMICS LTD
    公开号:WO2012155199A1
    公开(公告)日:2012-11-22
    The present invention relates to compounds useful in the modulation of potassium channel activity in cells, in particular the activity of Kv1.3 channels found in T cells. The invention also relates to the use of these compounds in the treatment or prevention of autoimmune and inflammatory diseases, including multiple sclerosis, pharmaceutical compositions containing these compounds and methods for their preparation.
    本发明涉及一种在细胞中调节钾通道活性的化合物,特别是发现在T细胞中的Kv1.3通道的活性。该发明还涉及利用这些化合物治疗或预防自身免疫和炎症性疾病,包括多发性硬化症,含有这些化合物的药物组合物以及其制备方法。
  • Amine derivatives
    申请人:Bionomics Limited
    公开号:EP2524912A1
    公开(公告)日:2012-11-21
    The present invention relates to Kv1.3 potassium channel blockers of Formula (I) and their use in the treatment of autoimmune and inflammatory diseases.
    本发明涉及公式(I)的Kv1.3钾通道阻滞剂及其在治疗自身免疫和炎症性疾病中的应用。
  • BORON-CONTAINING SMALL MOLECULES
    申请人:Baker Stephen J.
    公开号:US20090227541A1
    公开(公告)日:2009-09-10
    This invention provides, among other things, novel compounds useful for treating bacterial infections, pharmaceutical compositions containing such compounds, as well as combinations of these compounds with at least one additional therapeutically effective agent.
    本发明提供了用于治疗细菌感染的新型化合物,包括含有这些化合物的药物组合物,以及这些化合物与至少一种其他治疗有效剂的组合。
  • Amine Derivatives as Potassium Channel Blockers
    申请人:Harvey Andrew
    公开号:US20140336198A1
    公开(公告)日:2014-11-13
    The present invention relates to compounds useful in the modulation of potassium channel activity in cells, in particular the activity of Kv1.3 channels found in T cells. The invention also relates to the use of these compounds in the treatment or prevention of autoimmune and inflammatory diseases, including multiple sclerosis, pharmaceutical compositions containing these compounds and methods for their preparation.
    本发明涉及用于调节细胞中钾通道活性的化合物,特别是用于调节T细胞中发现的Kv1.3通道活性的化合物。本发明还涉及使用这些化合物治疗或预防自身免疫和炎症性疾病,包括多发性硬化症,含有这些化合物的制药组合物以及它们的制备方法。
  • 309. Benz-1 : 3-oxathioles, benz-1 : 4-oxathien, and αω-bisarylthioalkanes
    作者:Douglas Greenwood、Herbert A. Stevenson
    DOI:10.1039/jr9530001514
    日期:——
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同类化合物

四碘-2-磺基苯酸酐 四溴-2-磺基苯甲酸环酐 N,N'-二[[(1,3-苯并氧硫杂环戊烷-2-基)硫代]甲基]脲 5-羟基-4,6,7-三甲基-2-丙基-1,3-苯并氧杂噻唑 3-(5-羟基-4,6,7-三甲基-1,3-苯并氧杂噻唑-2-基)丙醇 2-磺基苯甲酸酐 2-(2-甲氧基丙烷-2-基)-7,7-二甲基-4-叔-丁基-8-氧杂-9-硫杂双环[4.3.0]壬-2,4,10-三烯 1,3-苯并噁噻唑,5-甲氧基-,3,3-二氧化 5,7-dimethyl-2-(2,2,2-trifluoro-1-methoxycarbonylethylidene)-1,3-benzooxathiole trans-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide trans-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide (2R,SS)-2-[(1S)-1-(4-methylphenyl)-1-(4-methoxyphenylamino)-methyl]-1,3-benzoxathiole 3(2H)-oxide 3,3-bis<(4-dimethylamino)phenyl>-4H-2,1-benzoxathiole 1-oxide 6-methyl-3,3-bis(4-dimethylaminophenyl)-3H-2,1-benzoxathiole 1-oxide (S)-6-(4-((R)-1-(5-ethylpyrimidin-2-yl)pyrrolidin-3-yl)methoxy-3-fluorophenyl)-2H-benzo[d][1,3]oxathiole 3-oxide 1,3-benzoxathiol-6-ol 1,3-benzoxathiol-6-ol-3-oxide 3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate 5-(5-t-butyldimethylsilyloxy-4,6,7-trimethyl-1,3-benzoxathiole-2-yl)-2,2-dimethylpentanoic acid trans-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide spiro<1,3-benzoxathiole-2,1'-cyclohexane> 3-oxide 4-Amino-3,3-dioxo-3λ6-benz[1,3]oxathiol-5-ol 6-Fluoro-1,3-benzoxathiol-2-amine 3H-2,1-Benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(2-ethoxyethoxy)ethoxy)ethoxy)- 4-[2-(4-Chloro-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-chloro-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-1,3-benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(4-chlorophenoxy)ethoxy)ethoxy)- 4-[2-(4-Methoxy-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-methoxy-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-2H-benzo[d][1,3]oxathiole 3,3-dioxide 4-(2-Methyl-benzo[1,3]dithiol-2-yl)-2-(2-methyl-benzo[1,3]oxathiol-2-yl)-1H-pyrrole 2,5-bis<2-(2-tert-butyl-1,3-benzoxathiolyl)>pyrrole 5-bromo-2-phenylbenzo[d][1,3]oxathiole 5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole 5-Ethoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 5-Butoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 2-t-Butyl-1,3-benzoxathiole 2-methyl-5'-nitrospiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 2,5'-dimethylspiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'-spirobi<3H-2,1-benzoxathiole> 1-oxide 3-imino-3H-2,1-benzoxathiole-1,1-dioxide Bis-(2-carboxyphenyl)-Schwefel-dihydroxid-dilacton 6-tert-Butyl-1,1,2a,4,4-pentamethyl-2a,4-dihydro-1H-2,3-dioxa-2aλ4-thia-cyclopenta[cd]indene 2,2-dimethyl-6-oxo-8-phenyl-2H,6H-<1,2>thioxolo<4,5,1-hi>benzthioxole 2-(5-Tert-butyl-3,3-dimethyl-2,1-benzoxathiol-7-yl)propan-2-ol 9-tert-Butyl-2,2,4,6,6-pentamethyl-3,5-dioxa-4λ4-thia-tricyclo[5.3.1.04,11]undeca-1(10),7(11),8-triene 4-oxide 2-(5-tert-Butyl-1-chloro-1,3,3-trimethyl-1,3-dihydro-1λ4-benzo[c][1,2]oxathiol-7-yl)-propan-2-ol