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(S)-N-[(2,6-dimethylphenoxy)ethyl]-2-aminopropan-1-ol | 1254734-12-7

中文名称
——
中文别名
——
英文名称
(S)-N-[(2,6-dimethylphenoxy)ethyl]-2-aminopropan-1-ol
英文别名
(S)-2-{[(2,6-dimethylphenoxy)ethyl]amino}propan-1-ol;S-(+)-2-([2-(2,6-dimethylphenoxy)ethyl]amino)-1-propanol;(2S)-2-[2-(2,6-dimethylphenoxy)ethylamino]propan-1-ol
(S)-N-[(2,6-dimethylphenoxy)ethyl]-2-aminopropan-1-ol化学式
CAS
1254734-12-7
化学式
C13H21NO2
mdl
——
分子量
223.315
InChiKey
SRNBWPJCLMSVQW-LBPRGKRZSA-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):
    1.9
  • 重原子数:
    16
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    41.5
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    丁二酸(S)-N-[(2,6-dimethylphenoxy)ethyl]-2-aminopropan-1-ol乙酸乙酯 为溶剂, 生成 bis{(S)-(+)-N-[2-(2,6-dimethylphenoxy)ethyl]-1-hydroxypropan-2-aminium} succinate
    参考文献:
    名称:
    1-羟基丙烷-2-氨基衍生物琥珀酸酯的超分子结构。
    摘要:
    氨基链烷醇和芳氧基烷基衍生物被称为潜在的抗惊厥药。两种新的盐,即双{(R,S)‐ N- [2-(2,6-二甲基苯氧基)乙基] -1-羟基丙烷-2-铵}琥珀酸盐(1s),C 13 H 22 NO 2 + ·0.5 C 4 H 4 O 4 2−和bis {(S)‐(+)‐ N‐ [2-(2,6-二甲基苯氧基)乙基] ‐1‐羟基丙烷‐2‐}}琥珀酸酯(2s),C 13 H 22 NO 2 + ·0.5C 4 H 4 O 4 2−通过单晶X射线衍射制备并表征。N原子通过从琥珀酸转移质子而质子化。盐1s在P 2 1 / n的空间群中以一个阳离子和一半阴离子在一个反对称中心上结晶,而(2s)在P 2 1的空间群中以四个阳离子和两个阴离子在非对称单元中结晶。。在两个R / S无序位置观察到1s阳离子的羟基。这两种盐的晶体显示出相似的超分子结构(即二维网络),主要由分子间的N + -H… Oδ-和O-H
    DOI:
    10.1107/s2053229618008574
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文献信息

  • DERIVATIVES OF AMINOALKANOLS, METHOD OF OBTAINING OF AMINOALKANOLS AND THEIR USE
    申请人:Marona Henryk
    公开号:US20110028562A1
    公开(公告)日:2011-02-03
    The subject of the invention is a group of new derivatives of aminoalkaπols, more specifically [(phenoxy)alkyl]aminoalkanols and [(phenoxy)acyl)aminoalkanols, their method of obtaining and their use for production of a medicine which is used in the prophylaxis, prevention and/or treatment of diseases or symptoms having neurological background and for production of a medicine with anticonvulsant activity, which is used in seizures of various origin, also in the limbic system, in myoclonic or sound-induced seizures, in psychomotor epilepsy, as well as in relieving neuropathic or inflammatory pain.
    本发明涉及一组新的氨基烷醇衍生物,更具体地是[(苯氧基)烷基]氨基烷醇和[(苯氧基)酰基)氨基烷醇,它们的获取方法以及它们用于生产用于预防、预防和/或治疗具有神经学背景的疾病或症状的药物,以及用于生产具有抗惊厥活性的药物,用于各种起源的癫痫发作,也用于边缘系统、肌阵挛或声音诱发的癫痫发作、精神运动性癫痫,以及缓解神经病性或炎症性疼痛。
  • US8633251B2
    申请人:——
    公开号:US8633251B2
    公开(公告)日:2014-01-21
  • US8841347B2
    申请人:——
    公开号:US8841347B2
    公开(公告)日:2014-09-23
  • [EN] DERIVATIVES OF AMINOALKANOLS, METHOD OF OBTAINING OF AMINOALKANOLS AND THEIR USE<br/>[FR] DÉRIVÉS D'AMINOALCANOLS, PROCÉDÉ D'OBTENTION D'AMINOALCANOLS ET LEUR UTILISATION
    申请人:UNIV JAGIELLONSKI
    公开号:WO2009093916A2
    公开(公告)日:2009-07-30
    The subject of the invention is a group of new derivatives of aminoalkaπols, more specifically [(phenoxy)alkyl]aminoalkanols and [(phenoxy)acyl)aminoalkanols, their method of obtaining and their use for production of a medicine which is used in the prophylaxis, prevention and/or treatment of diseases or symptoms having neurological background and for production of a medicine with anticonvulsant activity, which is used in seizures of various origin, also in the limbic system, in myoclonic or sound-induced seizures, in psychomotor epilepsy, as well as in relieving neuropathic or inflammatory pain.
  • Supramolecular architectures of succinates of 1-hydroxypropan-2-aminium derivatives
    作者:Ewa Żesławska、Wojciech Nitek、Henryk Marona、Anna M. Waszkielewicz
    DOI:10.1107/s2053229618008574
    日期:2018.7.1
    with four cations and two anions in the asymmetric unit. The hydroxy group of the cation of 1s is observed in two R/S disorder positions. The crystals of these two salts display similar supramolecular architectures (i.e. two‐dimensional networks), built mainly by intermolecular N+—H…Oδ− and O—H…Oδ− hydrogen bonds, where `δ−' represents a partial charge. The succinate anions are engaged in hydrogen
    氨基链烷醇和芳氧基烷基衍生物被称为潜在的抗惊厥药。两种新的盐,即双(R,S)‐ N- [2-(2,6-二甲基苯氧基)乙基] -1-羟基丙烷-2-铵}琥珀酸盐(1s),C 13 H 22 NO 2 + ·0.5 C 4 H 4 O 4 2−和bis (S)‐(+)‐ N‐ [2-(2,6-二甲基苯氧基)乙基] ‐1‐羟基丙烷‐2‐}}琥珀酸酯(2s),C 13 H 22 NO 2 + ·0.5C 4 H 4 O 4 2−通过单晶X射线衍射制备并表征。N原子通过从琥珀酸转移质子而质子化。盐1s在P 2 1 / n的空间群中以一个阳离子和一半阴离子在一个反对称中心上结晶,而(2s)在P 2 1的空间群中以四个阳离子和两个阴离子在非对称单元中结晶。。在两个R / S无序位置观察到1s阳离子的羟基。这两种盐的晶体显示出相似的超分子结构(即二维网络),主要由分子间的N + -H… Oδ-和O-H
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