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2-(2-Iodo-thiophen-3-yl)-ethanol | 187791-42-0

中文名称
——
中文别名
——
英文名称
2-(2-Iodo-thiophen-3-yl)-ethanol
英文别名
2-(2-Iodothiophen-3-yl)ethanol
2-(2-Iodo-thiophen-3-yl)-ethanol化学式
CAS
187791-42-0
化学式
C6H7IOS
mdl
——
分子量
254.091
InChiKey
NGZDENGIVJPWEA-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:
    293.2±25.0 °C(Predicted)
  • 密度:
    1.935±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    48.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

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文献信息

  • Development of synthetic routes to macrocyclic compounds based on the HSP90 inhibitor radicicol
    作者:Butrus Atrash、Tracey S. Cooper、Peter Sheldrake、Paul Workman、Edward McDonald
    DOI:10.1016/j.tetlet.2006.01.116
    日期:2006.3
    Short routes are reported to novel macrolides (e.g., 9, 12, 20) related to the HSP90 inhibitor radicicol.
    短路线被报告给新的大环内(例如,9,12,20)与所述HSP90抑制剂根赤壳菌素
  • [EN] NOVEL THIOPHENE COMPOUNDS FOR USE IN THERAPHY<br/>[FR] NOUVEAUX COMPOSÉS DU THIOPHÈNE THÉRAPEUTIQUES
    申请人:BIOCHROMIX PHARMA AB
    公开号:WO2010044743A1
    公开(公告)日:2010-04-22
    The present invention relates to novel substituted thiophene derivatives useful in therapy of diseases related to misfolded and aggregated proteins.
    本发明涉及新型取代噻吩生物,用于治疗与蛋白质错折和聚集相关的疾病。
  • Rapid Syntheses of Oligo(2,5-thiophene ethynylene)s with Thioester Termini:  Potential Molecular Scale Wires with Alligator Clips
    作者:Darren L. Pearson、James M. Tour
    DOI:10.1021/jo962335y
    日期:1997.3.1
    The syntheses of soluble oligo(3-ethyl-2,5-thiophene ethynylene)s via an iterative divergent/convergent approach starting from 3-ethyl-2-(trimethylsilylethynyl)thiophene are described. The monomer, dimer, tetramer, octamer, and 16-mer were synthesized. The 16-mer is 100 Angstrom long in its minimized extended zigzag conformation. At each stage in the iteration, the length of the framework doubles. Only three sets of reaction conditions are needed for the entire iterative synthetic sequence: an iodination, a protodesilylation, and a Pd/Cu-catalyzed cross coupling. The oligomers were characterized spectroscopically and by mass spectrometry. The optical properties are presented which show that at the octamer stage, the optical absorbance maximum is nearly saturated. The size exclusion chromatography values for the number average weights, relative to polystyrene, illustrate the tremendous differences in the hydrodynamic volume of these rigid rod oligomers verses the random coils of polystyrene. These differences become quite apparent at the octamer stage. Attachment of thiol end groups, protected as the thioacetyl moieties, was achieved. These serve as binding sites for adhesion to gold surfaces. In some cases, one end of the oligomeric chains were capped with a thiol group so that the surface attachments to gold could be studied. In other cases, thiol groups were affixed to both ends of the molecular chains so that future conduction studies could be done between proximal metallic probes. The rigid rod conjugated oligomers may act as molecular wires in molecular scale electronic devices, and they also serve as useful models for understanding analogous bulk polymers.
  • NOVEL THIOPHENE COMPOUNDS FOR USE IN THERAPHY
    申请人:CPL BCX PHARMA AB
    公开号:EP2350042B1
    公开(公告)日:2015-07-29
  • OLIGOTHIOPHENE DERIVATE AS MOLECULAR PROBES
    申请人:Celluminova AB
    公开号:EP2536712B1
    公开(公告)日:2015-03-18
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同类化合物

试剂2,5-Dibromo-3,4-dihexylthiophene 苯-1,2,4-三羧酸-丙烷-1,2,3-三醇(1:1) 碘吡咯 癸氯-二茂铁 甲酮,(4,5-二溴-1H-吡咯-2-基)苯基- 甲基3-氟-1H-1,2,4-三唑-5-羧酸酯 溴代二茂铁 溴-(3-溴-2-噻嗯基)镁 派瑞林D 派瑞林 F 二聚体 氯代二茂铁 曲洛酯 异噻唑,3-氯-5-甲基- 地茂酮 四碘硒吩 四碘噻吩 四碘呋喃 四溴噻吩 四溴吡咯 四溴-N-甲基吡咯 四氯噻吩 四氟噻吩 噻菌腈 噻美尼定. 噻吩,3-溴-4-(1-辛炔基)- 噻吩,3-溴-2-[2-(甲硫基)乙烯基]-,(Z)- 噻吩,3-溴-2-[2-(甲硫基)乙烯基]-,(E)- 噻吩,3-溴-2-[2-(甲硫基)乙烯基]-,(E)- 噻吩,2,5-二氯-3,4-二(氯甲基)- 喷贝特 咪唑烷,2-(4-溴-5-甲基-2-呋喃基)-1,3-二甲基- 叔丁基2-溴-4,6-二氢-5H-吡咯并[3,4-D]噻唑-5-羧酸酯 叔-丁基3-溴-6,7-二氢-1H-吡唑并[4,3-C]吡啶-5(4H)-甲酸基酯 叔-丁基2-溴-5,6-二氢咪唑并[1,2-A]吡嗪-7(8H)-甲酸基酯 叔-丁基(4-溴-5-氰基-1-甲基-1H-吡唑-3-基)氨基甲酯 双环[4.2.0]辛-1,3,5-三烯-7-甲腈,2-氟- 八氟联苯烯 八氟二苯并硒吩 全氟苯并环丁烯二酮 二苯基氯化碘盐 二联苯碘硫酸盐 二氯对二甲苯二聚体 二氯[2-甲基-3(2H)-异噻唑酮-O]的钙合物 二氯-1,2-二硫环戊烯酮 二-(3-溴-1,2,4-噻二唑-5-基)-二硫醚 二(2-噻吩基)碘鎓 乙酸,[[[1-(3-溴-5-异[口噁]唑基)亚乙基]氨基]氧代]-,甲基酯,(E)- [四丁基铵][Δ-三(四氯-1,2-苯二醇酸根)磷酸盐(V)] [3-(4-氯-3,5-二甲基-1H-吡唑-1-基)丙基]胺 [3-(4-氯-1H-吡唑-1-基)-2-甲基丙基]胺