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diisopropyl 3-aminophenylphosphonate | 89277-86-1

中文名称
——
中文别名
——
英文名称
diisopropyl 3-aminophenylphosphonate
英文别名
diisopropyl 3-anilinylphosphonate;Dipropan-2-yl(3-aminophenyl)phosphonate;3-di(propan-2-yloxy)phosphorylaniline
diisopropyl 3-aminophenylphosphonate化学式
CAS
89277-86-1
化学式
C12H20NO3P
mdl
——
分子量
257.269
InChiKey
QNVNIPSCYNQOGI-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

  • 熔点:
    103-104 °C
  • 沸点:
    368.7±25.0 °C(Predicted)
  • 密度:
    1.11±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    17
  • 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:
    61.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-Nitro-phenylphosphonsaeure-dichlorid 在 palladium on activated charcoal 氢气三乙胺 作用下, 以 甲醇二氯甲烷 为溶剂, 25.0 ℃ 、413.69 kPa 条件下, 反应 4.0h, 生成 diisopropyl 3-aminophenylphosphonate
    参考文献:
    名称:
    Phosphorus analogs of .gamma.-aminobutyric acid, a new class of anticonvulsants
    摘要:
    A series of phosphorus compounds, designed as analogues of gamma-aminobutyric acid (GABA) in that they possess a P = O moiety separated by three atoms from an amino or acetamido group, was synthesized and tested by using in vitro GABAA and GABAB receptor binding, GABA uptake assays, and was examined for anticonvulsant activity. Weak GABAB receptor affinity was noted for one agent, whereas six compounds displayed moderate to high potencies as inhibitors of electroshock- and pentylenetetrazol-induced seizures. The best anticonvulsant effect was found with the (m-aminophenyl) phosphinic acid compounds, with members of this class selected for further study.
    DOI:
    10.1021/jm00371a017
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文献信息

  • Palladium-Catalyzed Phosphorylation of Aryl Mesylates and Tosylates
    作者:Wai Chung Fu、Chau Ming So、Fuk Yee Kwong
    DOI:10.1021/acs.orglett.5b03104
    日期:2015.12.4
    The first general palladium catalyst for the phosphorylation of aryl mesylates and tosylates is reported. The newly developed system exhibits excellent functional group compatibility. For instance, free amino, keto, ester, and amido groups, as well as heterocycles, remain intact during the course of reaction. The mesylated derivatives of biologically active compounds such as 17β-estradiol and 6-hydroxyflavone
    据报道,第一种用于芳基甲磺酸酯和甲苯磺酸酯磷酸化的通用钯催化剂。新开发的系统具有出色的功能组兼容性。例如,游离氨基,酮,酯和酰胺基以及杂环在反应过程中保持完整。还显示了生物活性化合物(如17β-雌二醇和6-羟基黄酮)的甲磺酸化衍生物是适用的底物。描述了一种一锅磷酸化-氨基化序列,可轻松合成潜在的药效基团。
  • AMINO PYRIMIDINE ANTICANCER COMPOUNDS
    申请人:APPARI Rama Devi
    公开号:US20110136764A1
    公开(公告)日:2011-06-09
    Compounds of Formula 1, as shown below and defined herein: and pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancers mediated at least in part by FAK.
    以下为化学式1的化合物,本文中定义:以及其药学上可接受的盐、合成、中间体、制剂和治疗该疾病的方法,包括至少部分由FAK介导的癌症。
  • Amino pyrimidine anticancer compounds
    申请人:Appari Rama Devi
    公开号:US08399433B2
    公开(公告)日:2013-03-19
    Compounds of Formula 1, as shown below and defined herein: and pharmaceutically acceptable salts, synthesis, intermediates, formulations, and methods of disease treatment therewith, including cancers mediated at least in part by FAK.
    以下式子所示的化合物1及其药学上可接受的盐,合成、中间体、制剂和使用它们治疗疾病的方法,包括至少部分由FAK介导的癌症的治疗方法。
  • Revisiting the Hirao cross-coupling: improved synthesis of aryl and heteroaryl phosphonates
    作者:Yamina Belabassi、Saeed Alzghari、Jean-Luc Montchamp
    DOI:10.1016/j.jorganchem.2008.07.020
    日期:2008.9
    The palladium-catalyzed cross-coupling of dialkylphosphite with aromatic electrophiles (Hirao coupling) was re-investigated. Some limitations in terms of palladium loadings and substrate reactivity are alleviated with the use of Pd(OAc)(2) complexed to 1,1'-bis(diphenylphosphino) ferrocene (dppf) as a ligand. Various aryl and heteroaryl halides are employed to deliver both known and novel substituted phosphonates. The first examples of aryl chloride couplings are also reported. (C) 2008 Elsevier B.V. All rights reserved.
  • US8399433B2
    申请人:——
    公开号:US8399433B2
    公开(公告)日:2013-03-19
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