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(2S)-1-(4-chlorophenoxy)-3-(propan-2-ylamino)propan-2-ol

中文名称
——
中文别名
——
英文名称
(2S)-1-(4-chlorophenoxy)-3-(propan-2-ylamino)propan-2-ol
英文别名
——
(2S)-1-(4-chlorophenoxy)-3-(propan-2-ylamino)propan-2-ol化学式
CAS
——
化学式
C12H18ClNO2
mdl
——
分子量
243.733
InChiKey
JHNLCWKHEYGEHY-NSHDSACASA-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):
    2.3
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    41.5
  • 氢给体数:
    2
  • 氢受体数:
    3

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

点击查看最新优质反应信息

文献信息

  • Dynamic kinetic asymmetric synthesis of β-aminoalcohols from racemic epoxides in cyclodextrin complexes under solid state conditions
    作者:L. Rajender Reddy、N. Bhanumathi、K. Rama Rao
    DOI:10.1039/b004643o
    日期:——
    It has been shown for the first time that enantiopure β-aminoalcohols can be prepared from racemic epoxides by dynamic kinetic resolution involving enantio-differentiating racemisation in cyclodextrin complexes under solid state conditions.
    研究首次证明,在固态条件下,通过环糊精络合物中的对映体分化消旋化动态动力学解析,可从外消旋环氧化物制备出对映体纯δ-氨基丙醇。
  • Enantioselective ring opening of epoxides with trimethylsilyl azide (TMSN3) in the presence of β-cyclodextrin: an efficient route to 1,2-azido alcohols
    作者:Ahmed Kamal、M Arifuddin、Maddamsetty V Rao
    DOI:10.1016/s0957-4166(99)00464-4
    日期:1999.11
    The ring opening of epoxides with nucleophiles such as TMSN3 and isopropylamine takes place enantioselectively in the presence of (beta-cyclodextrin under extremely mild conditions and the azido alcohols and amino alcohols are formed as (S)-isomers. (C) 1999 Published by Elsevier Science Ltd. All rights reserved.
  • Enzyme catalyzed stereoselective synthesis of (S)-propanolamines
    作者:Ahmed Kamal、Maddamsetty V Rao
    DOI:10.1016/s0957-4166(00)86256-4
    日期:1994.10
    Stereoselective synthesis of (S)-propanolamines has been carried out by the ring opening of racemic epoxides with 2-propylamine in presence of lipases and subtilisin. The effect of solvent towards selectivity has also been studied.
  • Stereoselective synthesis of (S)-propanol amines: Lipase catalyzed opening of epoxides with 2-propylamine
    作者:Ahmed Kamal、Yalamati Damayanthi、Maddamsetty V. Rao
    DOI:10.1016/0957-4166(92)80006-i
    日期:1992.11
    The ring opening of epoxides with 2-propylamine in presence of lipase in organic solvents affords selectively (S)-propanol amines. The effect of solvents towards selectivity has also been examined.
  • Kamal Ahmed, Damayanthi Yalamati, Rao Maddamsetty V., Tetrahedron: Asymmetry, 3 (1992) N 11, S 1361-1364
    作者:Kamal Ahmed, Damayanthi Yalamati, Rao Maddamsetty V.
    DOI:——
    日期:——
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