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3,6-二苯氧基哒嗪 | 10340-55-3

中文名称
3,6-二苯氧基哒嗪
中文别名
哒嗪,3,6-二苯氧基-
英文名称
3,6-diphenoxypyridazine
英文别名
——
3,6-二苯氧基哒嗪化学式
CAS
10340-55-3
化学式
C16H12N2O2
mdl
——
分子量
264.283
InChiKey
JHDSLXBQHANMJH-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:
    140 °C
  • 沸点:
    435.4±30.0 °C(Predicted)
  • 密度:
    1.217±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    44.2
  • 氢给体数:
    0
  • 氢受体数:
    4

安全信息

  • 海关编码:
    2933990090

SDS

SDS:df094396c1678fa8d08dacbe53ea7bbd
查看

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:
    3,6-二苯氧基哒嗪奎宁环-3-醇potassium tert-butylate 作用下, 以 四氢呋喃 为溶剂, 反应 16.0h, 以45%的产率得到3-[(6-phenoxypyridazin-3-yl)oxy]quinuclidine
    参考文献:
    名称:
    3-Quinuclidinyl heteroatom bridged biaryl derivatives
    摘要:
    化合物的结构式(I)或其药学上可接受的盐、酰胺或前药,其中:n为0、1或2;X1为O、S、—N(R1)—、—N(Ar2)—和N(R2)C(O)—;Ar1为六元芳香环;Ar2为环己烷或根据本文定义的单环或双环芳香环。这些化合物可用于治疗由nAChR配体预防或缓解的疾病或疾病。还公开了具有结构式(I)化合物的药物组合物以及使用这些化合物和组合物的方法。
    公开号:
    US20050137398A1
  • 作为产物:
    描述:
    3-氯-6-苯氧基吡嗪苯酚potassium tert-butylate 作用下, 以 四氢呋喃 为溶剂, 反应 10.17h, 以84%的产率得到3,6-二苯氧基哒嗪
    参考文献:
    名称:
    3-Quinuclidinyl heteroatom bridged biaryl derivatives
    摘要:
    化合物的结构式(I)或其药学上可接受的盐、酰胺或前药,其中:n为0、1或2;X1为O、S、—N(R1)—、—N(Ar2)—和N(R2)C(O)—;Ar1为六元芳香环;Ar2为环己烷或根据本文定义的单环或双环芳香环。这些化合物可用于治疗由nAChR配体预防或缓解的疾病或疾病。还公开了具有结构式(I)化合物的药物组合物以及使用这些化合物和组合物的方法。
    公开号:
    US20050137398A1
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文献信息

  • Heilmittelchemische Studien in der heterocyclischen Reihe. 4. Mitteilung. Pyridazine I. Derivate des cyclischen Maleinsäure- und Citraconsäure-hydrazids
    作者:J. Druey、Kd. Meier、K. Eichenberger
    DOI:10.1002/hlca.19540370115
    日期:——
    A number of pyridazines and 4-methyl-pyridazines substituted in the 3- and 6-position are described for pharmacological investigations. Certain 3,6-dialkoxy-pyridazines have good anticonvulsive properties. The 3,6-dihydrazino-pyridazine resembles the blood pressure lowering drugs “A presoline” and “Nepresol” in its pharmacological properties. The sulfaderivative of 3-amino-6-chloro-pyridazine has excellent
    描述了许多3-和6-位取代的哒嗪和4-甲基哒嗪用于药理研究。某些3,6-二烷氧基-哒嗪具有良好的抗惊厥性质。3,6-二肼基哒嗪在其药理特性上类似于降血压药“ A presoline”和“ Nepresol”。3-氨基-6-氯哒嗪的磺基衍生物具有优异的抗菌作用。
  • 3-quinuclidinyl heteroatom bridged biaryl derivatives
    申请人:Abbott Laboratories
    公开号:US07241773B2
    公开(公告)日:2007-07-10
    Compounds of formula: or pharmaceutically acceptable salts, esters, amides, or prodrugs thereof, wherein: A and G are each independently N or N+—O−; m and n are each independently 0, 1, or 2; X1 and X3 are each independently O, S, and —N(R1)—; X2 is O, S, —N(R1)—, —N(Ar2)—and —N(R2)C(O)—; Ar1 is a six-membered aromatic ring; Ar2 is cyclohexyl or a mono- or bicyclic aromatic ring, and R13 is hydrogen, alkyl, or halogen, as defined herein. The compounds are useful in treating conditions or disorders prevented by or ameliorated by nAChR ligands. Also disclosed are pharmaceutical compositions having compounds of formulas (I) and (II) and methods for using such compounds and compositions.
    化合物的式子:或其药学上可接受的盐、酯、酰胺或前药,其中:A和G各自独立地为N或N+—O−;m和n各自独立地为0、1或2;X1和X3各自独立地为O、S和—N(R1)—;X2为O、S、—N(R1)—、—N(Ar2)—和—N(R2)C(O)—;Ar1为六元芳环;Ar2为环己基或单环或双环芳环,R13为氢、烷基或卤素,按照此处的定义。这些化合物在治疗由nAChR配体预防或缓解的疾病或疾病方面有用。还公开了具有式(I)和式(II)化合物的制药组合物及使用这种化合物和组合物的方法。
  • Itai; Igeta, Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1954, vol. 74, p. 1195,1197
    作者:Itai、Igeta
    DOI:——
    日期:——
  • Cyclometallated compounds. XIII. Cyclopalladation of 2-phenoxypyridine and structurally-related compounds
    作者:Duncan J de Geest、Brendan J O’Keefe、Peter J Steel
    DOI:10.1016/s0022-328x(98)01203-0
    日期:1999.5
    2-Phenoxypyridine and 2-phenylsulfanylpyridine are cyclopalladated readily by palladium acetate to give six-membered metallocycles. Extension to the three isomeric bis(2-pyridyloxy)benzenes leads to a new series of doubly-cyclopalladated compounds. In contrast, 3-6-diphenoxypyridazine and 4-6-diphenoxypyrimidine only undergo monopalladation, whilst their sulfur analogues are resistant to cyclopalladation. All cyclometallated compounds are converted to their acetylacetonate derivatives and the X-ray crystal structure of one of these is described. (C) 1999 Elsevier Science S.A. All rights reserved.
  • Process for Producing Olefin Copolymerization Catalyst and Process for Producing Olefin Copolymer
    申请人:NAKAHARA Shinya
    公开号:US20080227937A1
    公开(公告)日:2008-09-18
    A process for producing an olefin copolymerization catalyst, comprising the step of contacting, with one another, (A) a solid catalyst component containing a titanium atom, a magnesium atom and a halogen atom, (B) an organoaluminum compound and/or organoaluminumoxy compound, and (C) a nitrogen-containing aromatic heterocyclic compound, whose one or more carbon atoms adjacent to its nitrogen atom are linked to an electron-donating group, or a group containing an electron-donating group; and a process for producing an olefin copolymer using the an olefin copolymerization catalyst.
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