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N-Furfuryl-propylen-diamin-(1.3) | 21878-50-2

中文名称
——
中文别名
——
英文名称
N-Furfuryl-propylen-diamin-(1.3)
英文别名
N1-(2-Furylmethyl)-1,3-propanediamine;N'-(furan-2-ylmethyl)propane-1,3-diamine
N-Furfuryl-propylen-diamin-(1.3)化学式
CAS
21878-50-2
化学式
C8H14N2O
mdl
——
分子量
154.212
InChiKey
CJYLPHZWTNERHX-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):
    -0.2
  • 重原子数:
    11
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    51.2
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    糠醛1,3-丙二胺 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 生成 N-Furfuryl-propylen-diamin-(1.3)
    参考文献:
    名称:
    从硝基到肟的一个步骤:通过还原相应的乙烯基硝基化合物方便地制备不饱和肟
    摘要:
    可以通过相应的乙烯基硝基化合物通过SnCl 2 ·2H 2 O还原而方便地制备一系列新型不饱和肟。肟的结构通过1 H和13 C NMR,IR和HRMS以及X射线晶体学分析进行表征。 1-(6-氯-吡啶-3-基甲基)-4,5-二氢-1H-咪唑-2-甲醛甲醛肟2a表明,羟基以反式构型排列。简短调查的一些证据表明,这些肟似乎是由硝基脂族化合物的aci形式还原而形成的。
    DOI:
    10.1016/j.tet.2009.10.042
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文献信息

  • [EN] PROCESS FOR PREPARING GUANIDINO-FUNCTIONAL MONOMERS<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE MONOMÈRES À FONCTION GUANIDINO
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2014204763A1
    公开(公告)日:2014-12-24
    A process for preparing guanidino-functional, free radically polymerizable compounds comprises (a) combining (1) an amine compound comprising (i) at least one primary aliphatic amino group and (ii) at least one secondary aliphatic amino group, primary aromatic amino group, or secondary aromatic amino group, and (2) a guanylating agent; (b) allowing or inducing reaction of the amine compound and the guanylating agent to form a guanylated amine compound; (c) combining (1) the guanylated amine compound, and (2) a reactive monomer comprising (i) at least one ethylenically unsaturated group and (ii) at least one group that is reactive with an amino group; and (d) allowing or inducing reaction of the guanylated amine compound and the reactive monomer to form a guanidino-functional, free radically polymerizable compound.
    制备基功能自由基聚合化合物的过程包括(a)结合(1)包含(i)至少一个主链脂肪基团和(ii)至少一个次级链脂肪基团、主链芳香胺基团或次级芳香胺基团的胺基化合物和(2)基化试剂;(b)允许或诱导胺基化合物和基化试剂发生反应以形成基化胺基化合物;(c)结合(1)基化胺基化合物和(2)包含(i)至少一个乙烯不饱和基团和(ii)至少一个与基反应的基团的反应单体;(d)允许或诱导基化胺基化合物和反应单体发生反应以形成基功能自由基聚合化合物。
  • AMINOALCOHOL LIPIDOIDS AND USES THEREOF
    申请人:Mahon Kerry Peter
    公开号:US20110293703A1
    公开(公告)日:2011-12-01
    Aminoalcohol lipidoids are prepared by reacting an amine with an epoxide-terminated compound are described. Methods of preparing aminoalcohol lipidoids from commercially available starting materials are also provided. Aminoalcohol lipidoids may be prepared from racemic or stereochemically pure epoxides. Aminoalcohol lipidoids or salts forms thereof are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the amino moiety of these aminoalcohol lipidoid compounds, they are particularly suited for the delivery of polynucleotides. Complexes, micelles, liposomes or particles containing the inventive lipidoids and polynucleotide have been prepared. The inventive lipidoids may also be used in preparing microparticles for drug delivery. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings.
    本文描述了通过将胺与环氧末端化合物反应制备基醇脂质体的方法。还提供了从商业起始材料制备基醇脂质体的方法。基醇脂质体可以从外消旋或立体化学纯的环氧化合物制备。基醇脂质体或其盐形式最好是可生物降解和生物相容的,并可用于各种药物输送系统。鉴于这些基醇脂质体化合物的基基团,它们特别适用于多核苷酸的输送。已经制备了包含创新脂质体和多核苷酸的复合物、胶束、脂质体或粒子。创新脂质体也可以用于制备药物输送的微粒。鉴于它们能够缓冲其周围环境的pH值,它们在输送不稳定剂方面特别有用。
  • PROCESS FOR PREPARING GUANIDINO-FUNCTIONAL MONOMERS
    申请人:3M INNOVATIVE PROPERTIES COMPANY
    公开号:US20160096802A1
    公开(公告)日:2016-04-07
    A process for preparing guanidino-functional, free radically polymerizable compounds comprises (a) combining (1) an amine compound comprising (i) at least one primary aliphatic amino group and (ii) at least one secondary aliphatic amino group, primary aromatic amino group, or secondary aromatic amino group, and (2) a guanylating agent; (b) allowing or inducing reaction of the amine compound and the guanylating agent to form a guanylated amine compound; (c) combining (1) the guanylated amine compound, and (2) a reactive monomer comprising (i) at least one ethylenically unsaturated group and (ii) at least one group that is reactive with an amino group; and (d) allowing or inducing reaction of the guanylated amine compound and the reactive monomer to form a guanidino-functional, free radically polymerizable compound.
    制备含有基官能团、自由基聚合化合物的过程包括:(a)混合(1)一种胺化合物,该胺化合物包括(i)至少一个一级脂肪族基团和(ii)至少一个二级脂肪族基团、一级芳香族基团或二级芳香族基团,以及(2)一种基化试剂;(b)使胺化合物和基化试剂发生反应形成基化胺化合物;(c)混合(1)基化胺化合物和(2)一种反应单体,该反应单体包括(i)至少一个乙烯基不饱和基团和(ii)至少一个与基反应的基团;(d)使基化胺化合物和反应单体发生反应形成含有基官能团、自由基聚合化合物。
  • Process for preparing guanidino-functional monomers
    申请人:3M INNOVATIVE PROPERTIES COMPANY
    公开号:US10239828B2
    公开(公告)日:2019-03-26
    A process for preparing guanidino-functional, free radically polymerizable compounds comprises (a) combining (1) an amine compound comprising (i) at least one primary aliphatic amino group and (ii) at least one secondary aliphatic amino group, primary aromatic amino group, or secondary aromatic amino group, and (2) a guanylating agent; (b) allowing or inducing reaction of the amine compound and the guanylating agent to form a guanylated amine compound; (c) combining (1) the guanylated amine compound, and (2) a reactive monomer comprising (i) at least one ethylenically unsaturated group and (ii) at least one group that is reactive with an amino group; and (d) allowing or inducing reaction of the guanylated amine compound and the reactive monomer to form a guanidino-functional, free radically polymerizable compound.
    一种制备可自由基聚合的基官能团化合物的工艺包括(a)将(1)包含(i)至少一个伯脂族基和(ii)至少一个仲脂族基、伯芳族基或仲芳族基的胺化合物与(2)一种鸟苷酸化剂结合;(b)允许或诱导胺化合物与鸟苷酸化剂反应以形成鸟苷酸化胺化合物;(c) 将(1)鸟苷化胺化合物和(2)反应性单体结合,反应性单体包括(i)至少一个乙 烯不饱和基团和(ii)至少一个与基反应的基团;以及 (d) 允许或诱导鸟苷化胺化合物和反应性单体反应,以形成鸟苷酸官能团、可 自由基聚合的化合物。
  • Aminoalcohol lipidoids and uses thereof
    申请人:Massachusetts Institute of Technology
    公开号:US10189802B2
    公开(公告)日:2019-01-29
    Aminoalcohol lipidoids are prepared by reacting an amine with an epoxide-terminated compound are described. Methods of preparing aminoalcohol lipidoids from commercially available starting materials are also provided. Aminoalcohol lipidoids may be prepared from racemic or stereochemically pure epoxides. Aminoalcohol lipidoids or salts forms thereof are preferably biodegradable and biocompatible and may be used in a variety of drug delivery systems. Given the amino moiety of these aminoalcohol lipidoid compounds, they are particularly suited for the delivery of polynucleotides. Complexes, micelles, liposomes or particles containing the inventive lipidoids and polynucleotide have been prepared. The inventive lipidoids may also be used in preparing microparticles for drug delivery. They are particularly useful in delivering labile agents given their ability to buffer the pH of their surroundings.
    本文介绍了通过胺与环氧化物封端化合物反应制备基醇脂质的方法。还提供了从市售起始原料制备醇类脂质的方法。基醇脂质可由外消旋或立体化学环氧化物制备。醇类脂质或其盐类最好具有生物降解性和生物相容性,可用于各种给药系统。考虑到这些醇类脂化合物的基,它们特别适合用于多核苷酸的给药。现已制备出含有本发明类脂化合物和多核苷酸的复合物、胶束、脂质体或颗粒。本发明的类脂质还可用于制备给药微粒。由于本发明脂质具有缓冲周围环境 pH 值的能力,因此在递送易变药剂方面特别有用。
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