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3-isopropyl-5,5',6,6',7,7',8,8'-octahydro-2,2'-binapthol

中文名称
——
中文别名
——
英文名称
3-isopropyl-5,5',6,6',7,7',8,8'-octahydro-2,2'-binapthol
英文别名
2-(1-Hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)-3-propan-2-yl-5,6,7,8-tetrahydronaphthalen-1-ol
3-isopropyl-5,5',6,6',7,7',8,8'-octahydro-2,2'-binapthol化学式
CAS
——
化学式
C23H28O2
mdl
——
分子量
336.474
InChiKey
SDMIFIVGNYWHOK-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

计算性质

  • 辛醇/水分配系数(LogP):
    6.7
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.48
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthol三聚丙烯 以22%的产率得到3-isopropyl-5,5',6,6',7,7',8,8'-octahydro-2,2'-binapthol
    参考文献:
    名称:
    3-Alkylated-5,5',6,6',7,7,'8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and processes for making them
    摘要:
    揭示了组成物3-烷基化-5,5′,6,6′,7,7′,8,8′-辛氢-2,2′-联萘酚和3,3′-双烷基化-5,5′,6,6′,7,7′,8,8′-辛氢-2,2′-联萘酚,以及制备它们的各种方法,均涉及对5,5′,6,6′,7,7′,8,8′-辛氢-2,2′-联萘酚进行烷基化。
    公开号:
    US20030100803A1
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文献信息

  • 3 - Alkylated-5, 5',6, 6', 7, 7', 8, 8' - octahydro-2, 2' - binaphthols and 3, 3' - dialkylated- 5, 5', 6, 6', 7, 7', 8, 8' - octahydro - 2, 2' - binaphthols and processes for making
    申请人:Lu S. M. Helen
    公开号:US20050182279A1
    公开(公告)日:2005-08-18
    The compositions 3-alkylated-5,5′,6,6′,7,7′,8,8′-octahydro-2,2′-binaphthol and 3,3′-dialkylated-5,5′, 6,6′,7,7′,8,8′-octahydro-2,2′-binaphthol are disclosed, as well as various processes for making them, all involving the alkylation of 5,5′,6,6′,7,7′,8,8′-octahydro-2,2′-binaphthol.
    本文介绍了3-烷基化-5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚和3,3′-二烷基化-5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚的组成,以及制造它们的各种过程,都涉及对5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚进行烷基化。
  • 3-Alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated- 5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and processes for making them
    申请人:——
    公开号:US20040054237A1
    公开(公告)日:2004-03-18
    The compositions 3 -alkylated- 5,5′,6,6′,7,7′,8,8′ -octahydro- 2,2′ -binaphthol and 3,3′ -dialkylated- 5,5′,6,6′,7,7′,8,8′ -octahydro- 2,2′ -binaphthol are disclosed, as well as various processes for making them, all involving the alkylation of 5,5′,6,6′,7,7′,8,8′ -octahydro- 2,2′ -binaphthol.
    本发明公开了3-烷基化-5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚和3,3′-二烷基化-5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚,以及制备它们的各种方法,均涉及5,5′,6,6′,7,7′,8,8′-八氢-2,2′-联萘酚的烷基化。
  • 3-Alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'binaphthols and 3,3'-dialkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and process for making them
    申请人:E.I. du Pont de Nemours and Company
    公开号:EP1820790A2
    公开(公告)日:2007-08-22
    The composition 3-alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated- 5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols are disclosed, as well as various processes for making them, all involving the alkylation of 5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthol.
    3- 烷基化-5,5',6,6',7,7',8,8'-八氢-2,2'-联萘和 3,3'-二烷基化-5,5',6,6',7,7',8,8'-八氢-2、
  • 3-Alkylated-5,5',6,6',7,7',8,8'-Octahydro-2,2'-Binaphthols and 3,3'-Dialkylated-5,5',6,6',7,7',8,8'-Octahydro-2,2'-Binaphthols and processes for making them
    申请人:Invista Technologies S.à.r.l.
    公开号:EP2279994A1
    公开(公告)日:2011-02-02
    The composition 3-alkylated-5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols and 3,3'-dialkylated- 5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthols are disclosed, as well as various processes for making them, all involving the alkylation of 5,5',6,6',7,7',8,8'-octahydro-2,2'-binaphthol.
    3- 烷基化-5,5',6,6',7,7',8,8'-八氢-2,2'-联萘和 3,3'-二烷基化-5,5',6,6',7,7',8,8'-八氢-2、
  • Supported bis(phosphorus) ligands and their use in the catalysis
    申请人:——
    公开号:US20030153691A1
    公开(公告)日:2003-08-14
    Supported bis(phosphorus) ligands are disclosed for use in a variety of catalytic processes, including the isomerization, hydrogenation, hydroformylation, and hydrocyanation of unsaturated organic compounds. Catalysts are formed when the ligands are combined with a catalytically active metal, such as nickel.
    已公开的支撑双(磷)配体可用于各种催化过程,包括不饱和有机化合物的异构化、氢化、加氢甲酰化和加氢氰酸化。 当配体与催化活性金属(如镍)结合时,就形成了催化剂。
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