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4-(2-nitrophenoxy)-1,8-naphthalic anhydride | 111669-59-1

中文名称
——
中文别名
——
英文名称
4-(2-nitrophenoxy)-1,8-naphthalic anhydride
英文别名
6-(2-Nitrophenoxy)-1H,3H-naphtho[1,8-cd]pyran-1,3-dione;8-(2-nitrophenoxy)-3-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8,10-pentaene-2,4-dione
4-(2-nitrophenoxy)-1,8-naphthalic anhydride化学式
CAS
111669-59-1
化学式
C18H9NO6
mdl
——
分子量
335.273
InChiKey
WVAKQJWUJQLVEN-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):
    3.9
  • 重原子数:
    25
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    98.4
  • 氢给体数:
    0
  • 氢受体数:
    6

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

反应信息

  • 作为反应物:
    描述:
    4-(2-nitrophenoxy)-1,8-naphthalic anhydride盐酸铁粉溶剂黄146 、 sodium nitrite 作用下, 以 为溶剂, 反应 2.5h, 生成 苯并占吨酸酐
    参考文献:
    名称:
    氧杂环稠合萘二甲酰亚胺作为抗肿瘤剂的合成与生物学评价
    摘要:
    制备了三个系列的新颖的氧-杂环稠合的萘二甲酰亚胺衍生物(8a - 8f,13a - 13d,17a - 17d)。新合成的化合物及其硫杂环稠合的类似物(1a - 1c,2a - 2d,3a - 3c)显示出有效的抗增殖活性,与其结构密切相关。进一步的研究表明,所有代表性化合物13a,2a和17a,3a与阿莫那肽相似,它对topo II具有很强的抑制活性,并且对topo I的抑制作用也很强,以前很少报道过萘二甲酰亚胺衍生物。初步探索证明了他们的DNA序列偏好。总而言之,双重的topo I / topo II抑制作用和DNA序列优先选择可能有助于增强肿瘤的选择性并克服耐药性。
    DOI:
    10.1016/j.ejmech.2012.12.039
  • 作为产物:
    描述:
    1,8-萘二甲酸酐盐酸potassium permanganate磷酸 、 potassium hydroxide 、 sodium hydroxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 4.0h, 生成 4-(2-nitrophenoxy)-1,8-naphthalic anhydride
    参考文献:
    名称:
    The quest for highly fluorescent chromophores: evaluation of 1H,3H-isochromeno[6,5,4-mna]xanthene-1,3-dione (CXD)
    摘要:
    报道了强荧光染料1H,3H-异色喹诺[6,5,4-mna]黄色素-1,3-二酮(CXD)的光物理性质。
    DOI:
    10.1039/c4ra09728a
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文献信息

  • [EN] CYANATED BENZOXANTHENE AND BENZOTHIOXANTHENE COMPOUNDS<br/>[FR] COMPOSÉS DE BENZOXANTHÈNE ET DE BENZOTHIOXANTHÈNE CYANATÉS
    申请人:BASF SE
    公开号:WO2016151068A1
    公开(公告)日:2016-09-29
    The present invention relates to cyanated compounds of the formula (I) wherein at least one of the radicals R2, R3, R4 and R5 is CN, and the remaining radicals are selected from hydrogen, chlorine and bromine; X is O, S, SO or SO2; m is 0, 1, 2, 3 or 4; R1 is selected from bromine, chlorine, cyano, -NRaRb, C1-C24-alkyl, C1-C24-haloalkyl, C1-C24-alkoxy, C1-C24-haloalkoxy, C3-C24-cycloalkyl, heterocycloalkyl, heteroaryl, C6-C24-aryl, C6-C24-aryloxy, C6-C24-aryl-C1-C10-alkylene, etc.; A is a diradical selected from diradicals of the general formulae (A.1), (A.2), (A.3), and (A.4) (A.1) (A.2) (A.3) (A.4) wherein R6, (R7)n, (R8)o and (R9)p are as defined in the claims and in the description. The invention further relates to color converters comprising at least one polymer as a matrix material and at least one cyanated compound of formula (I) or mixtures thereof as a fluorescent dye, to the use of the color converters and to lighting devices comprising at least one LED and at least one color converter.
    本发明涉及公式(I)的氰化合物,其中R2、R3、R4和R5中至少一个基团为CN,其余基团选自氢、氯和溴;X为O、S、SO或SO2;m为0、1、2、3或4;R1选自溴、氯、氰基、-NRaRb、C1-C24-烷基、C1-C24-卤代烷基、C1-C24-烷氧基、C1-C24-卤代烷氧基、C3-C24-环烷基、杂环烷基、杂芳基、C6-C24-芳基、C6-C24-芳氧基、C6-C24-芳基-C1-C10-烷基等;A为从一般公式(A.1)、(A.2)、(A.3)和(A.4)中选择的双基团(A.1)(A.2)(A.3)(A.4),其中R6、(R7)n、(R8)o和(R9)p如权利要求和描述中所定义。本发明还涉及包含至少一种聚合物作为基质材料和至少一种公式(I)的氰化合物或其混合物作为荧光染料的颜色转换剂,以及使用颜色转换剂和包含至少一种LED和至少一种颜色转换剂的照明设备。
  • CLASS OF GREEN/YELLOW EMITTING PHOSPHORS BASED ON DERIVATIVES OF BENZIMIDAZOXANTHENOISOQUINOLINONE FOR LED LIGHTING
    申请人:Philips Lighting Holding B.V.
    公开号:US20160264860A1
    公开(公告)日:2016-09-15
    The invention provides a lighting device ( 1 ) comprising (a) a light source ( 10 ) configured to generate light source light ( 11 ), and (b) a light converter ( 100 ) configured to convert at least part of the light source light ( 11 ) into visible converter light ( 111 ), wherein the light converter ( 100 ) comprises a matrix ( 120 ) containing a luminescent material ( 140 ) based on derivatives of benzimidazoxanthenoisoquinolinone. The lighting device may further comprise a further luminescent material ( 130 ).
    本发明提供了一种照明装置(1),包括(a)配置为产生光源光(11)的光源(10),以及(b)配置为将至少部分光源光(11)转换为可见转换器光(111)的光转换器(100),其中光转换器(100)包括一个基于苯并咪唑氧茚异喹啉酮衍生物的荧光材料(140)的矩阵(120)。该照明装置还可以包括另一种荧光材料(130)。
  • Cyanated benzoxanthene and benzothioxanthene compounds
    申请人:BASF SE
    公开号:US10125143B2
    公开(公告)日:2018-11-13
    Disclosed herein are cyanated compounds of the formula (I) wherein at least one of the radicals R2, R3, R4 and R5 is CN, and the remaining radicals are selected from hydrogen, chlorine and bromine; X is O, S, SO or SO2; m is 0, 1, 2, 3 or 4; R1 is selected from bromine, chlorine, cyano, —NRaRb, C1-C24-alkyl, C1-C24-haloalkyl, C1-C24-alkoxy, C1-C24-haloalkoxy, C3-C24-cycloalkyl, heterocycloalkyl, heteroaryl, C6-C24-aryl, C6-C24-aryloxy, C6-C24-aryl-C1-C10-alkylene, etc.; A is a diradical selected from diradicals of the general formulae (A.1), (A.2), (A.3), and (A.4) wherein R6, (R7)n, (R8)o and (R9)p are as defined in the claims and in the description. Also disclosed are color converters containing at least one polymer as a matrix material and at least one cyanated compound of formula (I) or mixtures thereof as a fluorescent dye, the use of the color converters, and lighting devices containing an LED and at least one color converter.
    本文公开了式 (I) 的氰基化合物,其中 R2、R3、R4 和 R5 中至少有一个基团是 CN,其余基团选自氢、氯和溴;X 是 O、S、SO 或 SO2;m 是 0、1、2、3 或 4;R1 选自溴、氯、氰基、-NRaRb、C1-C24-烷基、C1-C24-卤代烷基、C1-C24-烷氧基、C1-C24-卤代烷氧基、C3-C24-环烷基、杂环烷基、杂芳基、C6-C24-芳基、C6-C24-芳氧基、C6-C24-芳基-C1-C10-烯基等。A 是选自通式 (A.1)、(A.2)其中 R6、(R7)n、(R8)o 和 (R9)p 如权利要求和说明中所定义。还公开了含有至少一种聚合物作为基体材料和至少一种式(I)氰化化合物或其混合物作为荧光染料的颜色转换器、颜色转换器的用途以及含有发光二极管和至少一种颜色转换器的照明设备。
  • Benzoxanthene-3,4-dicarboximides and benzimidazoxanthenoisoquinolinones
    作者:Xuhong Qian、Shengwu Ren
    DOI:10.1021/je00054a038
    日期:1988.10
  • Novel aliphatic N-oxide of naphthalimides as fluorescent markers for hypoxic cells in solid tumor
    作者:Hong Yin、Weiping Zhu、Yufang Xu、Min Dai、Xuhong Qian、Yuanli Li、Jianwen Liu
    DOI:10.1016/j.ejmech.2011.04.040
    日期:2011.7
    A series of novel aliphatic N-oxide of naphthalimides (A1-A5) were designed and prepared. The N-O group was firstly introduced into the amine side chain tailed to planar naphthalimide chromophore as hypoxic bioreductive marker. Fluorescence image analysis showed that the compounds could be used as potential markers for hypoxic cells (V79) in vitro especially for A1 with 17 times hypoxic-oxic fluorescence differential, which was probably due to the bis-bioreduction mechanism. (C) 2011 Elsevier Masson SAS. All rights reserved.
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