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1-(5,6-二氢-萘-1-基)-乙酮 | 802918-49-6

中文名称
1-(5,6-二氢-萘-1-基)-乙酮
中文别名
——
英文名称
1-(5,6-dihydro-naphthalen-1-yl)-ethanone
英文别名
1-(5,6-dihydronaphthalen-1-yl)-ethanone;1-(5,6-Dihydronaphthalen-1-yl)ethanone
1-(5,6-二氢-萘-1-基)-乙酮化学式
CAS
802918-49-6
化学式
C12H12O
mdl
——
分子量
172.227
InChiKey
UXVYXDBJXVOYQQ-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:
    305.4±31.0 °C(Predicted)
  • 密度:
    1.069±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-(5,6-二氢-萘-1-基)-乙酮titanium(IV) isopropylate 、 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 生成 西那卡特杂质7
    参考文献:
    名称:
    Synthesis of Cinacalcet congeners
    摘要:
    Two racemic isomeric dihydronaphthalenes 1 and 2 were prepared from commercially available 5-hydroxytetralone in five linear steps. A key palladium-catalyzed double bond migration led to the synthesis of both isomers from the same starting material. Preparative chiral HPLC separation provided the enantiomerically pure materials. An asymmetric synthesis employing CBS reduction to furnish 1 was also developed. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.09.063
  • 作为产物:
    描述:
    1,5-二羟基-1,2,3,4-四氢萘 在 palladium diacetate 、 1,3-双(二苯基膦)丙烷三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 16.0h, 生成 1-(5,6-二氢-萘-1-基)-乙酮
    参考文献:
    名称:
    Synthesis of Cinacalcet congeners
    摘要:
    Two racemic isomeric dihydronaphthalenes 1 and 2 were prepared from commercially available 5-hydroxytetralone in five linear steps. A key palladium-catalyzed double bond migration led to the synthesis of both isomers from the same starting material. Preparative chiral HPLC separation provided the enantiomerically pure materials. An asymmetric synthesis employing CBS reduction to furnish 1 was also developed. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2004.09.063
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文献信息

  • Dihydronaphthalene compounds, compositions, uses thereof, and methods for synthesis
    申请人:Amgen Inc.
    公开号:US07361789B1
    公开(公告)日:2008-04-22
    The present invention relates to novel dihydronaphthalene compounds, compositions, methods for using the same, and processes for preparing the same. The present invention also relates to novel total synthesis approaches for preparing these compounds. In addition, the present invention relates to methods of producing quantities of isomers of these compounds and separating and purifying them using chiral separation techniques. The present invention also relates to methods of producing quantities of a single isometric compound without the need for chiral separation techniques.
    本发明涉及新颖的二氢萘烯化合物、组合物、使用方法以及制备这些化合物的方法。本发明还涉及用于制备这些化合物的新型全合成方法。此外,本发明涉及生产这些化合物的异构体的方法,并利用手性分离技术对其进行分离和纯化。本发明还涉及生产单一立体异构体化合物的方法,无需使用手性分离技术。
  • US7361789B1
    申请人:——
    公开号:US7361789B1
    公开(公告)日:2008-04-22
  • Synthesis of Cinacalcet congeners
    作者:Xin Wang、Ying Chen、Richard Crockett、Jorge Briones、Tony Yan、Carlos Orihuela、Benxin Zhi、John Ng
    DOI:10.1016/j.tetlet.2004.09.063
    日期:2004.11
    Two racemic isomeric dihydronaphthalenes 1 and 2 were prepared from commercially available 5-hydroxytetralone in five linear steps. A key palladium-catalyzed double bond migration led to the synthesis of both isomers from the same starting material. Preparative chiral HPLC separation provided the enantiomerically pure materials. An asymmetric synthesis employing CBS reduction to furnish 1 was also developed. (C) 2004 Elsevier Ltd. All rights reserved.
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