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Chinolin-2-phosphonsaeure | 14646-14-1

中文名称
——
中文别名
——
英文名称
Chinolin-2-phosphonsaeure
英文别名
2-quinolinephosphonic acid;Quinolin-2-ylphosphonic acid
Chinolin-2-phosphonsaeure化学式
CAS
14646-14-1
化学式
C9H8NO3P
mdl
——
分子量
209.141
InChiKey
SEYSHJHUAAIPDL-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):
    0.1
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    70.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    dysprosium(III) nitrate hexahydrate 、 zinc(II) sulfate heptahydrateChinolin-2-phosphonsaeure硫酸 作用下, 以 为溶剂, 反应 48.0h, 以60%的产率得到β-Dy(2-quinolinehydrogenphosphonato)(SO4)(H2O)2
    参考文献:
    名称:
    pH-controlled polymorphism in a layered dysprosium phosphonate and its impact on the magnetization relaxation
    摘要:
    这篇论文报告了两种多态的镝化合物,它们表现出不同的磁化缓慢松弛能垒。
    DOI:
    10.1039/c4cc09341k
  • 作为产物:
    描述:
    3,4-二氢-2(1H)-喹啉酮盐酸三氯氧磷 作用下, 以 为溶剂, 反应 12.33h, 生成 Chinolin-2-phosphonsaeure
    参考文献:
    名称:
    磷酰氯促使苯并内酰胺与亚磷酸三乙酯反应,得到苯并环化的单膦酸酯,而不是预期的双膦酸酯
    摘要:
    相比于脂族内酰胺,这给了环状aminomethylene-宝石-bisphosphonates在反应中与亚磷酸三乙酯和磷酰氯,相应的内酰胺benzoannulated通常提供可变的结构,这取决于基片的脂肪族环的大小的monophosphonates。它们很可能是通过双膦酸酯的去膦酰基化而获得的,双膦酸酯是该反应的初始产物。这些膦酸酯在酸水解和储存时似乎不稳定。已经提出了酸催化这些化合物降解的机理。
    DOI:
    10.1016/j.jorganchem.2015.03.005
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文献信息

  • Microbiocidal process employing full quaternary nitrogen-heterocyclic
    申请人:Petrolite Corporation
    公开号:US04101654A1
    公开(公告)日:1978-07-18
    Quaternary nitrogen-heterocyclic phosphonates wherein the phosphonate group is ortho- or para- to the nitrogen heterocyclic group, where the compounds are characterized as follows: ##STR1## WHEREIN THE DOTTED LINE REPRESENTS A CYCLIC STRUCTURE WHICH CYCLIC STRUCTURE MAY BE THE SOLE CYCLIC STRUCTURE, OR MAY BE ATTACHED TO OTHER CYCLIC GROUPS, WHERE R is a hydrocarbon or a substituted hydrocarbon group such as alkyl, aryl, alkaryl, aralkyl, etc., and X is an anion such as halogen, a sulfite, a sulfate, s sulfonate-containing group, etc. These nitrogen-heterocyclic phosphonates are prepared by reacting an aromatic nitrogen-heterocyclic compound, wherein the nitrogen atom is in the form of a quaternary alkoxy derivative (N-OR hereinafter defined) with a phosphite salt, preferably in the form of an ester of the phosphite, as exemplified by the following equation: ##STR2## Quaternaries of these compounds are prepared by further reaction with a quaternizing agent. These compounds which may be characterized as quaternaries of phosphonates of nitrogen-heterocyclics have many uses including their use as biocides, such as bacteriocides, herbicides, corrosion inhibitors, chelating agents, etc.
    四元氮杂环膦酸盐,其中膦酸盐基团位于氮杂环基团的邻位或对位,该化合物的特征如下:##STR1## 其中虚线表示环状结构,该环状结构可以是唯一的环状结构,也可以连接其他环状基团。其中,R是烃或取代烃基团,例如烷基,芳基,烷基芳基,芳基烷基等,X是阴离子,例如卤素,亚硫酸盐,硫酸盐,含磺酸盐基团等。这些氮杂环膦酸盐是通过将芳香性氮杂环化合物与膦酸盐反应制备而成,其中氮原子以四元烷氧衍生物(N-OR,下称)的形式存在,膦酸盐最好是膦酸盐酯的形式,例如以下方程式:##STR2## 这些化合物的四元盐可通过进一步与四元化试剂反应制备而成。这些化合物可被描述为氮杂环膦酸盐的四元盐,具有许多用途,包括作为生物杀菌剂,如细菌杀菌剂,除草剂,防腐剂,螯合剂等。
  • LIPID CLEAVAGE ENZYME
    申请人:——
    公开号:US20020106363A1
    公开(公告)日:2002-08-08
    A membranous enzyme not yet described in the state-of-the-art can be extracted from cellular membrane fractions of blood leukocytes or monocytes/macrophages. Also disclosed is the use of substrates of this enzyme to prepare medicaments that contain these substrates as pharmaceutical active substance. These medicaments are useful to direct pharmacologically active substances to target cells and to enrich target cells with said substances. Also disclosed are in-vitro research systems containing this enzyme used to detect other substrates of this enzyme.
    一种尚未在现代技术中描述的膜酶可以从血液白细胞或单核/巨噬细胞的细胞膜分离物中提取。还公开了使用该酶底物制备含有这些底物作为药物活性成分的药物的用途。这些药物可用于将药理活性物质定向到目标细胞并用该物质富集目标细胞。还公开了含有该酶的体外研究系统,用于检测该酶的其他底物。
  • Polymorphic Lanthanide Phosphonates Showing Distinct Magnetic Behavior
    作者:Dai Zeng、Min Ren、Song-Song Bao、Zhong-Sheng Cai、Chang Xu、Li-Min Zheng
    DOI:10.1021/acs.inorgchem.6b00280
    日期:2016.6.6
    A series of layered lanthanide phosphonates α-Ln(2-qpH)(SO4)(H2O)2 (α-Ln; Ln = Gd, Tb, Ho, Er) and β-Ln(2-qpH)(SO4)(H2O)2 (β-Ln; Ln = Gd, Tb, Ho, Er, Yb) (2-qpH2 = 2-quinolinephosphonic acid) have been synthesized and characterized. Compounds α-Ln crystallize in monoclinic space group P21/c, while compounds β-Ln crystallize in triclinic space group P1̅. Magnetic studies reveal that dominant ferromagnetic
    一系列层状镧系元素膦酸酯α-Ln(2-qpH)(SO 4)(H 2 O)2(α-Ln ; Ln = Gd,Tb,Ho,Er)和β-Ln(2-qpH)(SO 4)(H 2 O)2(β-Ln; Ln = Gd,Tb,Ho,Er,Yb)(2-qpH 2 = 2-喹啉膦酸)已合成并表征。化合物α-Ln在单斜空间群P 2 1 / c中结晶,而化合物β-Ln在三斜空间群P中结晶1̅。磁性研究表明,在所有情况下,主要的铁磁相互作用都在磁性中心之间传播。在化合物β-Er和β-Yb中观察到磁场诱导的磁弛豫。
  • Layered lanthanide phosphonates Ln(2-qpH)(SO<sub>4</sub>)(H<sub>2</sub>O)<sub>2</sub> (Ln = La, Ce, Pr, Nd, Sm): polymorphism and magnetic properties
    作者:Xiu-Fang Ma、Dai Zeng、Chang Xu、Song-Song Bao、Li-Min Zheng
    DOI:10.1039/d3dt01698f
    日期:——
    and interlayer interactions on their magnetic dynamics. Herein we report a series of layered lanthanide phosphonates, namely, α-Ln(2-qpH)(SO4)(H2O)2 (Ln = Sm) (α-Ln), β-Ln(2-qpH)(SO4)(H2O)2 (Ln = Pr, Nd, Sm) (β-Ln) and γ-Ln(2-qpH)(SO4)(H2O)2 (Ln = La, Ce, Pr, Nd, Sm) (γ-Ln) (2-qpH2 = 2-quinolinephosphonic acid), which crystallize in monoclinic P21/c (α-Ln), triclinic P (β-Ln) and orthorhombic Pbca
    多晶型层状稀土配位聚合物提供了研究层内和层间相互作用对其磁动力学影响的机会。在此,我们报道了一系列层状镧系膦酸盐,即α-Ln(2-qpH)(SO 4 )(H 2 O) 2 (Ln = Sm) ( α-Ln ), β-Ln(2-qpH)( SO 4 )(H 2 O) 2 (Ln = Pr, Nd, Sm) ( β-Ln ) 和 γ-Ln(2-qpH)(SO 4 )(H 2 O) 2 (Ln = La, Ce, Pr , Nd, Sm) ( γ-Ln ) (2-qpH 2 = 2-喹啉膦酸),结晶为单斜晶系P 2 1 / c ( α-Ln )、三斜晶系P ( β-Ln ) 和斜方晶系Pbca ( γ- ln ) 空间群,分别。β相和γ相的结构差异不仅存在于层内,而且存在于层间。在层内,Ln 2 O 2二聚体在β相中平行排列,但在γ相中不平行。在层间,α相和β相的喹啉基团之间存在π-π相互作用,
  • Lapid cleavage enzyme
    申请人:Heidelberg Pharma Holding GmbH
    公开号:US20030082167A1
    公开(公告)日:2003-05-01
    A membranous enzyme not yet described in the state-of-the-art can be extracted from cellular membrane fractions of blood leukocytes or monocytes/macrophages. Also disclosed is the use of substrates of this enzyme to prepare medicaments that contain these substrates as pharmaceutical active substance. These medicaments are useful to direct pharmacologically active substances to target cells and to enrich target cells with said substances. Also disclosed are in-vitro research systems containing this enzyme used to detect other substrates of this enzyme.
    可以从血液白细胞或单核细胞/巨噬细胞的细胞膜分馏物中提取一种尚未在最新技术中描述的膜酶。 还公开了利用这种酶的底物制备含有这些底物作为药用活性物质的药物。 这些药剂可将药理活性物质导向靶细胞,并用上述物质富集靶细胞。 还公开了含有这种酶的体外研究系统,用于检测这种酶的其它底物。
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