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1-(2-methoxy-[1,1'-biphenyl]-4-yl)ethanone | 56917-30-7

中文名称
——
中文别名
——
英文名称
1-(2-methoxy-[1,1'-biphenyl]-4-yl)ethanone
英文别名
1-(3-methoxy-4-phenyl)phenylethanone;3'-methoxy-4'-phenylacetophenone;1-(2-Methoxy[1,1a(2)-biphenyl]-4-yl)ethanone;1-(3-methoxy-4-phenylphenyl)ethanone
1-(2-methoxy-[1,1'-biphenyl]-4-yl)ethanone化学式
CAS
56917-30-7
化学式
C15H14O2
mdl
——
分子量
226.275
InChiKey
HUCGHZJCTDHMQE-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:
    326.7±22.0 °C(Predicted)
  • 密度:
    1.076±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 下游产品
    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:
    1-(2-methoxy-[1,1'-biphenyl]-4-yl)ethanone 在 palladium on activated charcoal 氢溴酸氢气 作用下, 以 溶剂黄146乙酸乙酯 为溶剂, 生成 4-(1-甲基乙基)[1,1'-联苯]-2-醇
    参考文献:
    名称:
    FR2231393
    摘要:
    公开号:
  • 作为产物:
    描述:
    1-(4-溴-3-甲氧基苯基)乙酮苯硼酸 在 bis-triphenylphosphine-palladium(II) chloride 、 caesium carbonate 作用下, 以 1,4-二氧六环 为溶剂, 反应 22.0h, 以98%的产率得到1-(2-methoxy-[1,1'-biphenyl]-4-yl)ethanone
    参考文献:
    名称:
    Structure-Based Approach to the Development of Potent and Selective Inhibitors of Dihydrofolate Reductase from Cryptosporidium
    摘要:
    Cryptosporidiosis is an emerging infectious disease that can be life-threatening in ail immune-compromised individual and causes gastrointestinal distress lasting up to 2 weeks in an immune-competent individual. There are few therapeutics available for effectively treating this disease. We have been exploring dihydrofolate reductase (DHFR) as a potential target in Cryptosporidium. On the basis of the structure of the DHFR enzyme from C. hominis, we have developed a novel scaffold that led to the discovery of potent (38 nM) and efficient inhibitors of this enzyme. Recently, we have advanced these inhibitors to the next stage of development. Using the Structures of both the protozoal and human enzymes. we have developed inhibitors with nanomolar potency (1.1 nM) against the pathogenic enzyme and high levels (1273-fold) of selectivity over the human enzyme.
    DOI:
    10.1021/jm8009124
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文献信息

  • An efficient palladium–benzimidazolyl phosphine complex for the Suzuki–Miyaura coupling of aryl mesylates: facile ligand synthesis and metal complex characterization
    作者:Kin Ho Chung、Chau Ming So、Shun Man Wong、Chi Him Luk、Zhongyuan Zhou、Chak Po Lau、Fuk Yee Kwong
    DOI:10.1039/c2cc15972d
    日期:——
    A new class of easily accessible hemilabile benzimidazolyl phosphine ligands has been developed. The ligand skeleton is prepared from commercially available and inexpensive o-phenylenediamine and 2-bromobenzoic acid. With catalyst loading down to 0.5 mol% palladium, excellent catalytic activity towards the Suzuki-Miyaura coupling of aryl mesylates is still observed. This represents the lowest catalyst
    已经开发出一种新型的易于获得的半不稳定的苯并咪唑基膦配体。配体骨架由可商购的和廉价的邻苯二胺和2-溴苯甲酸制备。在催化剂负载量低至0.5mol%钯的情况下,仍观察到对甲磺酸甲磺酸酯的Suzuki-Miyaura偶联的优异催化活性。通常,这代表了迄今为止该反应所达到的最低催化剂负载量。X射线晶体学表明,新的配体L2以Kappa(2)-P,N的方式与Pd配合。
  • Palladium-catalyzed Buchwald-Hartwig Amination and Suzuki-Miyaura Cross-coupling Reaction of Aryl Mesylates
    作者:Shun Wong
    DOI:10.15227/orgsyn.092.0195
    日期:——
  • A General Palladium-Catalyzed Suzuki-Miyaura Coupling of Aryl Mesylates
    作者:Chau Ming So、Chak Po Lau、Fuk Yee Kwong
    DOI:10.1002/anie.200803193
    日期:2008.10.6
  • Ligands for transition-metals and methods of use
    申请人:Kwong Fuk Yee
    公开号:US20090326243A1
    公开(公告)日:2009-12-31
    The present invention relates to indolyl phosphine ligands, and methods of making such ligands utilizing phenyl hydrazines and aryl ketones as the starting material. The present invention further includes uses of the ligands in the synthesis of pharmaceuticals, materials, and agriculture.
  • US3991212A
    申请人:——
    公开号:US3991212A
    公开(公告)日:1976-11-09
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