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2-(2-adamantyl)ethyl methanesutfonate | 151620-62-1

中文名称
——
中文别名
——
英文名称
2-(2-adamantyl)ethyl methanesutfonate
英文别名
2-(2-Adamantyl)ethyl methanesulfonate;2-(2-adamantyl)ethyl methanesulfonate
2-(2-adamantyl)ethyl methanesutfonate化学式
CAS
151620-62-1
化学式
C13H22O3S
mdl
——
分子量
258.382
InChiKey
PNKDCWDMBNEQQQ-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):
    3.3
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    51.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    2-(2-adamantyl)ethyl methanesutfonate四(三苯基膦)钯 、 sodium carbonate 、 caesium carbonate 作用下, 以 N,N-二甲基甲酰胺甲苯 为溶剂, 反应 22.0h, 生成 2''''',3''''''-Bis-(2-adamantan-2-yl-ethoxy)-4-methoxy-2',2'',2''',2''''-tetramethyl-[1,1';4',4'';1'',1''';4''',4'''';1'''',1''''';4''''',1'''''']septiphenyl
    参考文献:
    名称:
    Synthesis of asymmetric septi-(p-phenylene)s
    摘要:
    In this Letter, we describe the synthesis of two amphiphilic septi(p-phenylene)s, One terminus of each rigid-rod scaffold is linked through a spacer to a hydrophilic IDA-subunit, the two benzenes at the other terminus carry hydrophobic substituents of different size. These synthetic receptor models are expected to mimic biological processes that occur at cell membranes. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)01041-7
  • 作为产物:
    描述:
    2-(adamantan-2-yl)ethan-1-ol甲基磺酰氯三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 0.08h, 以93%的产率得到2-(2-adamantyl)ethyl methanesutfonate
    参考文献:
    名称:
    Synthesis of asymmetric septi-(p-phenylene)s
    摘要:
    In this Letter, we describe the synthesis of two amphiphilic septi(p-phenylene)s, One terminus of each rigid-rod scaffold is linked through a spacer to a hydrophilic IDA-subunit, the two benzenes at the other terminus carry hydrophobic substituents of different size. These synthetic receptor models are expected to mimic biological processes that occur at cell membranes. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)01041-7
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文献信息

  • DERIVATIVES OF 4-(2-AMINO-1-HYDROXYETHYL)PHENOL AS AGONISTS OF THE BETA2 ADRENERGIC RECEPTORS
    申请人:Giulio Matassa Victor
    公开号:US20100324000A1
    公开(公告)日:2010-12-23
    The present disclosure relates to 4-(2-amino-1-hydroxyethyl)phenol derivatives of formula (I) as well as pharmaceutical compositions comprising them, and their use in therapy as agonists of the β2 adrenergic receptor.
    本公开涉及公式(I)的4-(2-氨基-1-羟乙基)苯酚衍生物,以及包含它们的制药组合物,以及它们作为β2肾上腺素能受体激动剂在治疗中的应用。
  • US8178679B2
    申请人:——
    公开号:US8178679B2
    公开(公告)日:2012-05-15
  • Synthesis of asymmetric septi-(p-phenylene)s
    作者:Bereket Ghebremariam、Stefan Matile
    DOI:10.1016/s0040-4039(98)01041-7
    日期:1998.7
    In this Letter, we describe the synthesis of two amphiphilic septi(p-phenylene)s, One terminus of each rigid-rod scaffold is linked through a spacer to a hydrophilic IDA-subunit, the two benzenes at the other terminus carry hydrophobic substituents of different size. These synthetic receptor models are expected to mimic biological processes that occur at cell membranes. (C) 1998 Elsevier Science Ltd. All rights reserved.
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