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3-aminopropyl morpholine | 749801-06-7

中文名称
——
中文别名
——
英文名称
3-aminopropyl morpholine
英文别名
3-Morpholinpropylamine;3-morpholin-3-ylpropan-1-amine
3-aminopropyl morpholine化学式
CAS
749801-06-7
化学式
C7H16N2O
mdl
MFCD19214550
分子量
144.217
InChiKey
PFDDBXPXNRGYDV-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:
    238.2±15.0 °C(Predicted)
  • 密度:
    0.953±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.7
  • 重原子数:
    10
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    47.3
  • 氢给体数:
    2
  • 氢受体数:
    3

文献信息

  • BENZIMIDAZOLE AND IMADAZOPYRIDINE CARBOXIMIDAMIDE COMPOUNDS
    申请人:Gilead Sciences, Inc.
    公开号:US20160333009A1
    公开(公告)日:2016-11-17
    The present disclosure provides indoleamine 2,3-dioxygenase 1 (IDOL) inhibitors of Formula I: or pharmaceutically acceptable salts thereof, in which X, L, n, m, R 1 , R 2a , R 2b , R n , R m , and R t are as defined herein, as well as pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts thereof, and methods of using the same to treat conditions mediated by IDO1.
    本公开提供了式I的吲哌酮2,3-二氧化酶1(IDOL)抑制剂: 或其药学上可接受的盐,其中X、L、n、m、R 1 、R 2a 、R 2b 、R n 、R m 和R t 如本文所定义,以及包括式I化合物的药物组合物,或其药学上可接受的盐,并使用这些方法来治疗由IDO1介导的疾病。
  • ANTIVIRAL COMPOUNDS
    申请人:Aktoudianakis Evangelos
    公开号:US20100022508A1
    公开(公告)日:2010-01-28
    The invention is related to anti-viral compounds, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.
    这项发明涉及抗病毒化合物,含有这种化合物的组合物,以及包括给予这种化合物的治疗方法,还涉及用于制备这种化合物的过程和中间体。
  • Biaryl Amino Acids and Their Use in Dna Binding Oligomers
    申请人:Howard Wilson Philip
    公开号:US20070249591A1
    公开(公告)日:2007-10-25
    Compounds of formula (1): Z′-CO-A-B—NH-Z (I) wherein: Z is H or an amino protecting group; Z′ is OH, a protected or activated hydroxyl group or Cl; A is an optionally substituted C 5-6 arylene group; and B is an optionally substituted C 5-6 arylene group.
    公式(1)的化合物:Z'-CO-A-B—NH-Z(I),其中:Z为H或保护基;Z'为OH,受保护或活化羟基或Cl;A为可选取代的C5-6芳基烃基;B为可选取代的C5-6芳基烃基。
  • BIARYL AMINO ACIDS AND THEIR USE IN DNA BINDING OLIGOMERS
    申请人:Howard Philip Wilson
    公开号:US20110160192A1
    公开(公告)日:2011-06-30
    Compounds of formula (I): Z′-CO-A-B—NH-Z (I) wherein: Z is H or an amino protecting group; Z′ is OH, a protected or activated hydroxyl group or Cl; A is an optionally substituted C 5-6 arylene group; and B is an optionally substituted C 5-6 arylene group.
    化合物的化学式(I):Z'-CO-A-B—NH-Z (I),其中:Z为氢或基保护基;Z'为OH,受保护或活化的羟基或Cl;A为可选取代的C5-6芳基烃基;B为可选取代的C5-6芳基烃基。
  • Rapid generation of diverse nucleoside and nucleotide libraries
    申请人:——
    公开号:US20020051991A1
    公开(公告)日:2002-05-02
    Methods for generation of nucleoside libraries are provided in which nucleosides or nucleoside precursors (e.g., a sugar or a base) are coupled to a solid phase and sequentially reacted with various substrates.
    提供了生成核苷文库的方法,其中核苷或核苷前体(如糖或碱)与固相耦合,并依次与各种底物反应。
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