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4-nitroso-4'-methoxydiphenylamine | 7696-66-4

中文名称
——
中文别名
——
英文名称
4-nitroso-4'-methoxydiphenylamine
英文别名
N-(4-methoxyphenyl)-4-nitrosoaniline
4-nitroso-4'-methoxydiphenylamine化学式
CAS
7696-66-4
化学式
C13H12N2O2
mdl
——
分子量
228.25
InChiKey
QTJWGXNCAKOQSC-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:
    390.6±27.0 °C(Predicted)
  • 密度:
    1.15±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    50.7
  • 氢给体数:
    1
  • 氢受体数:
    4

SDS

SDS:01edcb247fd63da769c9fece6ebc61bc
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Novel Imaging Agents for Detecting Neurological Dysfunction
    申请人:Kolb Hartmuth C.
    公开号:US20110046378A1
    公开(公告)日:2011-02-24
    Disclosed here in are compounds and methods of diagnosing Alzheimer's Disease or a predisposition thereto in a mammal, the method comprising administering to the mammal a diagnostically effective amount of a radiolabeled compound, wherein the compound is selected from the group consisting of radiolabeled flavones, coumarins, carbazoles, quinolinones, chromenones, imidazoles and triazoles derivatives, allowing the compound to distribute into the brain tissue, and imaging the brain tissue, wherein an increase in binding of the compound to the brain tissue compared to a normal control level of binding indicates that the mammal is suffering from or is at risk of developing Alzheimer's Disease
    本文披露了一种诊断哺乳动物阿尔茨海默病或其易感性的化合物和方法,该方法包括向哺乳动物施用诊断有效量的放射性标记化合物,所述化合物选自放射性标记的黄酮类、香豆素类、咔唑类、喹啉酮类、香豆素酮类、咪唑类和三唑类衍生物组,使化合物分布到脑组织中,并成像脑组织,其中与正常结合水平相比,化合物与脑组织的结合增加表明该哺乳动物正在患有或有发展阿尔茨海默病的风险。
  • p-Nitrosophenol chemistry. II. Amination of p-nitrosophenol ethers with primary aromatic amines
    作者:John T. Hays、Herbert Lewis Young、Herbert H. Espy
    DOI:10.1021/jo01277a039
    日期:1967.1
  • Molecular-Level Insight into the Differential Oxidase and Oxygenase Reactivities of <i>de Novo</i> <i>Due Ferri</i> Proteins
    作者:Rae Ana Snyder、Susan E. Butch、Amanda J. Reig、William F. DeGrado、Edward I. Solomon
    DOI:10.1021/jacs.5b03524
    日期:2015.7.29
    Using the single-chain due ferri (DFsc) peptide scaffold, the differential oxidase and oxygenase reactivities of two 4A -> 4G variants, one with two histidines at the diiron center (G4DFsc) and the other with three histidines (3His-G4DFsc(Mut3)), are explored. By controlling the reaction conditions, the active form responsible for 4-aminophenol (4-AP) oxidase activity in both G4DFsc and 3His-G4DFsc(Mut3) is determined to be the substrate-bound biferrous site. Using circular dichroism (CD), magnetic CD (MCD), and variable-temperature, variable-field (VTVH) MCD spectroscopies, 4-AP is found to bind directly to the biferrous sites of the DF proteins. In G4DFsc, 4-AP increases the coordination of the biferrous site, while in 3His-G4DFsc(Mut3), the coordination number remains the same and the substrate likely replaces the additional bound histidine. This substrate binding enables a two-electron process where 4-AP is oxidized to benzoquinone imine and O-2 is reduced to H2O2. In contrast, only the biferrous 3His variant is found to be active in the oxygenation of p-anisidine to 4-nitroso-methoxybenzene. From CD, MCD, and VTVH MCD, p-anisidine addition is found to minimally perturb the biferrous centers of both G4DFsc and 3His-G4DFsc(Mut3), indicating that this substrate binds near the biferrous site. In 3His-G4DFsc(Mut3), the coordinative saturation of one iron leads to the two-electron reduction of O-2 at the second iron to generate an end-on hydroperoxo-Fe(III) active oxygenating species.
  • Mizhiritskii, M. D.; Kuz'min, S. V.; Kogan, L. M., Journal of Organic Chemistry USSR (English Translation), 1989, vol. 25, # 6.2, p. 1204 - 1205
    作者:Mizhiritskii, M. D.、Kuz'min, S. V.、Kogan, L. M.
    DOI:——
    日期:——
  • MIZHIRITSKIJ, M. D.;KUZMIN, S. V.;KOGAN, L. M., ZH. ORGAN. XIMII, 25,(1989) N, S. 1340-1341
    作者:MIZHIRITSKIJ, M. D.、KUZMIN, S. V.、KOGAN, L. M.
    DOI:——
    日期:——
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