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1-[α-(4-methoxy-benzylidenamino)-benzyl]-[2]naphthol | 97035-64-8

中文名称
——
中文别名
——
英文名称
1-[α-(4-methoxy-benzylidenamino)-benzyl]-[2]naphthol
英文别名
1-[[(4-Methoxyphenyl)methylideneamino]-phenylmethyl]naphthalen-2-ol
1-[α-(4-methoxy-benzylidenamino)-benzyl]-[2]naphthol化学式
CAS
97035-64-8
化学式
C25H21NO2
mdl
——
分子量
367.447
InChiKey
HUIQEPMQCKTSJG-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):
    5.7
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    41.8
  • 氢给体数:
    1
  • 氢受体数:
    3

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

  • 作为反应物:
    描述:
    1-[α-(4-methoxy-benzylidenamino)-benzyl]-[2]naphthol碘苯二乙酸 作用下, 以 甲醇 为溶剂, 以75%的产率得到3-(4-methoxyphenyl)-1-phenyl-1H-benzo[f][1,3]benzoxazine
    参考文献:
    名称:
    Synthesis, antimicrobial and cytotoxicity study of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines
    摘要:
    A series of new 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines (3 and 7) was synthesized in good yields and the structure was determined with the help of NMR, 2D-NMR, HRMS studies and X-ray crystallography. These compounds were tested in vitro for their antibacterial activity against Gram-positive and Gram-negative bacteria and as well as for antifungal activity. The compounds 3c, 3e, 7a, 7d and 7k showed significant antibacterial activity and 71 showed moderate antifungal activity. The cytotoxicity of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines showed that 3e and 7e are more effective against breast, lung and colon cell proliferation. (C) 2012 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2012.08.018
  • 作为产物:
    参考文献:
    名称:
    Synthesis, antimicrobial and cytotoxicity study of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines
    摘要:
    A series of new 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines (3 and 7) was synthesized in good yields and the structure was determined with the help of NMR, 2D-NMR, HRMS studies and X-ray crystallography. These compounds were tested in vitro for their antibacterial activity against Gram-positive and Gram-negative bacteria and as well as for antifungal activity. The compounds 3c, 3e, 7a, 7d and 7k showed significant antibacterial activity and 71 showed moderate antifungal activity. The cytotoxicity of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines showed that 3e and 7e are more effective against breast, lung and colon cell proliferation. (C) 2012 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2012.08.018
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文献信息

  • Impact of the initial doses of rocuronium and pancuronium on subsequent maintenance for neuromuscular block
    作者:Steven E. Kern、Robert J. Fragen、Paul C. Fitzgerald、Michiel van Zeeland、Joel O. Johnson
    DOI:10.1007/bf03019724
    日期:2001.2
    Purpose: To determine the impact of the neuromuscular blocking agent given for intubation on the duration of effect of multiple maintenance doses of pancuronium and rocuronium.Methods: Seventy-eight subjects were randomly assigned to receive one of four dosing combinations for intubation and neuromuscular maintenance: rocuronium for intubation and maintenance, rocuronium for intubation and pancuronium for maintenance, pancuronium for intubation and rocuronium for maintenance, or pancuronium for both. Each time that the first twitch response returned to 25% of the baseline value, the duration of the dose was determined and another maintenance dose was administered. The duration of action of the maintenance doses was compared between the groups.Results: Twitch suppression from the first maintenance dose was shorter for subjects who received rocuronium for both doses (Group RR) compared with that for subjects that received pancuronium (Groups PR & PP) as their intubation dose ( 17.6 vs 34 & 59.8 min, respectively, P < 0.05). Subjects who received rocuronium followed by pancuronium (Group RP) showed a shorter duration of twitch suppression after the first maintenance dose than the group that received pancuronium for both doses (Group PP) (21.3 vs 59.8 min, P < 0.05). By the third maintenance dose. the influence of the intubating dose on the maintenance dose duration had essentially diminished.Conclusions: For combinations of rocuronium and pancuronium, the duration of twitch suppression after a maintenance dose is only dependent on the first agent given for the first two maintenance doses administered.
  • Desai, N.C.; Shukla, H.K.; Langalia, N.A., Journal of the Indian Chemical Society, 1984, vol. 61, p. 711 - 713
    作者:Desai, N.C.、Shukla, H.K.、Langalia, N.A.、Thaker, K.A.
    DOI:——
    日期:——
  • Betti, Gazzetta Chimica Italiana, 1907, vol. 37 I, p. 63,64
    作者:Betti
    DOI:——
    日期:——
  • Synthesis, antimicrobial and cytotoxicity study of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines
    作者:Vikas Verma、Kuldeep Singh、Devinder Kumar、Thomas M. Klapötke、Jörg Stierstorfer、Balasubramanian Narasimhan、Asif Khurshid Qazi、Abid Hamid、Sundeep Jaglan
    DOI:10.1016/j.ejmech.2012.08.018
    日期:2012.10
    A series of new 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines (3 and 7) was synthesized in good yields and the structure was determined with the help of NMR, 2D-NMR, HRMS studies and X-ray crystallography. These compounds were tested in vitro for their antibacterial activity against Gram-positive and Gram-negative bacteria and as well as for antifungal activity. The compounds 3c, 3e, 7a, 7d and 7k showed significant antibacterial activity and 71 showed moderate antifungal activity. The cytotoxicity of 1,3-disubstituted-1H-naphtho[1,2-e][1,3]oxazines showed that 3e and 7e are more effective against breast, lung and colon cell proliferation. (C) 2012 Elsevier Masson SAS. All rights reserved.
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