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2,3-环氧-1,4-苯醌 | 15254-69-0

中文名称
2,3-环氧-1,4-苯醌
中文别名
——
英文名称
benzoquinoepoxide
英文别名
2,3-epoxy-1,4-benzoquinone;2,5-Dioxo-7-oxa-bicyclo<4.1.0>hepten-(3);Chinonoxid;5,6-epoxy-cyclohex-2-ene-1,4-dione;7-Oxabicyclo[4.1.0]hept-3-ene-2,5-dione
2,3-环氧-1,4-苯醌化学式
CAS
15254-69-0
化学式
C6H4O3
mdl
——
分子量
124.096
InChiKey
XQUCGJMSQRPJEX-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):
    -0.4
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    46.7
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2932999099

SDS

SDS:46e208b3d821a9e384788838ef3372df
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反应信息

  • 作为反应物:
    描述:
    2,3-环氧-1,4-苯醌甲基三苯基溴化膦lithium diisopropyl amide 作用下, 以 四氢呋喃 为溶剂, 反应 0.75h, 以39%的产率得到3,6-dimethylidene-1,2-epoxy-4-cyclohexene
    参考文献:
    名称:
    A New Catalytic and Enantioselective Desymmetrization of Symmetrical Methylidene Cycloalkene Oxides
    摘要:
    [GRAPHICS]Chiral copper complexes of C-2-symmetrical phosphoroamidites were found to be highly effective catalysts for both kinetic resolution and novel desymmetrization reactions of new methylidene epoxycycloalkanes.
    DOI:
    10.1021/ol005584o
  • 作为产物:
    参考文献:
    名称:
    A New Catalytic and Enantioselective Desymmetrization of Symmetrical Methylidene Cycloalkene Oxides
    摘要:
    [GRAPHICS]Chiral copper complexes of C-2-symmetrical phosphoroamidites were found to be highly effective catalysts for both kinetic resolution and novel desymmetrization reactions of new methylidene epoxycycloalkanes.
    DOI:
    10.1021/ol005584o
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文献信息

  • Competitive epoxidation and quinone formation in the dimethyldioxirane oxidation of diazoquinones as ambident nucleophiles
    作者:Waldemar Adam、Lazaros Hadjiarapoglou、Karsten Mielke、Alexander Treiber
    DOI:10.1016/s0040-4039(00)77264-9
    日期:1994.8
    In addition to the expected dimethyldioxirane (DMD) oxidation of diazoquinones 1 to their quinones 2, the corresponding epoxy quinones 3 are formed directly and not as secondary overoxidation products of the quinones 2 since the latter are persistent towards DMD under these conditions; this novel oxidation is rationalized in terms of the ambident nucleophilic nature of the diazoquinones and corroborated
    除了重氮醌1预期的二甲基二环氧乙烷(DMD)氧化成其醌2外,相应的环氧醌3是直接形成的,而不是醌2的二次过氧化产物,因为后者在这些条件下对DMD具有持久性。根据重氮醌的亲核性质合理地解释了这种新颖的氧化反应,并通过MO(AM1)计算得到了证实。
  • HKOCl-2 Series of Green BODIPY-Based Fluorescent Probes for Hypochlorous Acid Detection and Imaging in Live Cells
    作者:Jun Jacob Hu、Nai-Kei Wong、Qiangshuai Gu、Xiaoyu Bai、Sen Ye、Dan Yang
    DOI:10.1021/ol501496n
    日期:2014.7.3
    A HKOCl-2 series of new fluorescent probes for hypochlorous acid (HOCl) detection in live cells is reported. The probes exhibit excellent selectivity, sensitivity, and chemostability toward HOCl. In particular, HKOCl-2b rapidly and selectively detects endogenous HOCl in both human and mouse macrophages. These probes could therefore serve as promising discovery tools to help elucidate biological functions
    报道了用于活细胞中次氯酸(HOCl)检测的HKOCl-2系列新荧光探针。探针表现出优异的选择性,灵敏度和对HOCl的化学稳定性。特别地,HKOC1-2b迅速且选择性地检测人和小鼠巨噬细胞中的内源性HOCl。因此,这些探针可以用作有希望的发现工具,以帮助阐明HOC1的生物学功能。
  • Quinone Substituted Quinazoline and Quinoline Kinase Inhibitors
    申请人:Floyd Jr Brawner Middleton
    公开号:US20070299092A1
    公开(公告)日:2007-12-27
    The present invention provides for compounds with the general formula: A compound of formula (1) having the structure (1) wherein Z is a radical selected from the group (a), (b), or (c) as well as methods and compositions containing these compounds useful for treatment of diseases that are characterized, at least in part, by excessive, abnormal, or inappropriate angiogenesis. These disease states, include but are not limited to, cancer, diabetic retinopathy, macular degeneration and rheumatoid arthritis. These compounds inhibit angiogenesis by inhibiting a tyrosine kinase receptor enzyme, specifically KDR, and binding to the KDR in an irreversible manner.
    本发明提供了一般式为:具有结构式(1)的化合物,其中Z是从(a)、(b)或(c)组中选择的基团,以及包含这些化合物的方法和组合物,用于治疗至少部分特征为过度、异常或不适当血管生成的疾病。这些疾病状态包括但不限于癌症、糖尿病视网膜病变、黄斑变性和类风湿性关节炎。这些化合物通过抑制酪氨酸激酶受体酶,特别是KDR,并以不可逆的方式与KDR结合来抑制血管生成。
  • Dual-color HIV reporter system for the detection of latently-infected cells
    申请人:THE J. DAVID GLADSTONE INSTITUTES
    公开号:US10106818B2
    公开(公告)日:2018-10-23
    The present disclosure provides for recombinant nucleic acids, and cells and virions comprising the recombinant nucleic acids, that can be used to identify, isolate, and/or purify cells latently infected with immunodeficiency virus. A subject recombinant nucleic acid includes (a) a first nucleotide sequence encoding a first reporter polypeptide that produces a first detectable signal, where the first nucleotide sequence is operably linked to an immunodeficiency virus promoter and is translated as an early gene; and (b) a second nucleotide sequence encoding a second reporter polypeptide that produces a second detectable signal that is distinguishable from the first detectable signal, where the second nucleotide sequence is operably linked to a non-immunodeficiency virus promoter. In some aspects, the first and second nucleotide sequences are both positioned between a shared 5′ long terminal repeat (LTR) and a shared 3′ LTR. Also provided are related methods.
    本公开提供了重组核酸以及包含重组核酸的细胞和病毒,可用于鉴定、分离和/或纯化潜伏感染免疫缺陷病毒的细胞。受试重组核酸包括:(a) 第一核苷酸序列,编码产生第一检测信号的第一报告基因多肽,其中第一核苷酸序列与免疫缺陷病毒启动子可操作连接,并作为早期基因翻译;(b) 编码第二报告基因多肽的第二核苷酸序列,它产生的第二检测信号与第一检测信号不同,其中第二核苷酸序列与非免疫缺陷病毒启动子可操作地连接。在某些方面,第一和第二核苷酸序列都位于共享的 5′长末端重复序列(LTR)和共享的 3′长末端重复序列(LTR)之间。还提供了相关的方法。
  • Coxon, James M.; O'Connell, Michael J.; Steel, Peter J., Australian Journal of Chemistry, 1986, vol. 39, # 10, p. 1537 - 1557
    作者:Coxon, James M.、O'Connell, Michael J.、Steel, Peter J.
    DOI:——
    日期:——
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