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(1S)-7-甲氧基-1-甲基-1,2,3,4-四氢异喹啉-6-醇盐酸盐 | 881-26-5

中文名称
(1S)-7-甲氧基-1-甲基-1,2,3,4-四氢异喹啉-6-醇盐酸盐
中文别名
——
英文名称
(-)-Salsoline hydrochloride
英文别名
(+)-salsoline hydrochloride;(S)-7-methoxy-1-methyl-1,2,3,4-tetrahydro-isoquinolin-6-ol; hydrochloride;(S)-7-Methoxy-1-methyl-1,2,3,4-tetrahydro-isochinolin-6-ol; Hydrochlorid;(-)-S-salsoline hydrochloride;(1S)-7-methoxy-1-methyl-1,2,3,4-tetrahydroisoquinolin-6-ol;hydrochloride
(1S)-7-甲氧基-1-甲基-1,2,3,4-四氢异喹啉-6-醇盐酸盐化学式
CAS
881-26-5
化学式
C11H15NO2*ClH
mdl
——
分子量
229.707
InChiKey
PZZVNEZKNWRZEG-FJXQXJEOSA-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

  • 熔点:
    147-149 °C

计算性质

  • 辛醇/水分配系数(LogP):
    -2.41
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    46.1
  • 氢给体数:
    2
  • 氢受体数:
    3

SDS

SDS:bc86358590728dc900d736f40ef88f02
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反应信息

  • 作为产物:
    参考文献:
    名称:
    Study of chiral β-enaminones prepared from pyrrolidine, cytisine, salsoline and 2-amino-1-(4-nitrophenyl)propane-1,3-diol: resolution of salsoline via diastereomeric modified carane-type β-enaminones
    摘要:
    A series of novel optically active beta-enaminones have been prepared regio- and stereoselectively from primary and secondary amines (pyrrolidine, cytisine salsoline and 2-amino-l-(4-nitrophenyl)propane-1,3-diol) and (+)-3-carene-derived beta-chlorovinyl ketone. Resolution of the isoquinoline alkaloid salsoline has been demonstrated as well as isolation of a single diastereomeric adduct from racemic 2-amino-1-(4-nitrophenyl)propane-1,3-diol. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0957-4166(02)00781-4
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文献信息

  • Study of chiral β-enaminones prepared from pyrrolidine, cytisine, salsoline and 2-amino-1-(4-nitrophenyl)propane-1,3-diol: resolution of salsoline via diastereomeric modified carane-type β-enaminones
    作者:Sergey A. Popov、Yuri V. Gatilov、Tatjana V. Rybalova、Alexey V. Tkachev
    DOI:10.1016/s0957-4166(02)00781-4
    日期:2003.1
    A series of novel optically active beta-enaminones have been prepared regio- and stereoselectively from primary and secondary amines (pyrrolidine, cytisine salsoline and 2-amino-l-(4-nitrophenyl)propane-1,3-diol) and (+)-3-carene-derived beta-chlorovinyl ketone. Resolution of the isoquinoline alkaloid salsoline has been demonstrated as well as isolation of a single diastereomeric adduct from racemic 2-amino-1-(4-nitrophenyl)propane-1,3-diol. (C) 2003 Elsevier Science Ltd. All rights reserved.
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