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Salicylaldehyd-selenosemicarbazon | 17222-65-0

中文名称
——
中文别名
——
英文名称
Salicylaldehyd-selenosemicarbazon
英文别名
N'-[(2-hydroxyphenyl)methylideneamino]carbamimidoselenoic acid
Salicylaldehyd-selenosemicarbazon化学式
CAS
17222-65-0
化学式
C8H9N3OSe
mdl
——
分子量
242.139
InChiKey
HHTISYBTBPNJNJ-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:
    391.9±44.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.47
  • 重原子数:
    13.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    70.64
  • 氢给体数:
    3.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    trans-bis(triphenylphosphine)palladium dichloride 、 Salicylaldehyd-selenosemicarbazon 在 Et3N 作用下, 以 甲苯 为溶剂, 以63%的产率得到
    参考文献:
    名称:
    环己酮硒亚氨基甲酰胺:方便的原料,用于制备官能化硒亚氨基甲酮及其Pt和Pd配合物
    摘要:
    在环己酮存在下,水合肼与KSeCN在酸性乙醇水溶液中反应,可得到高产率的环己酮硒亚氨基卡巴carb。通过用醛处理,将环己酮硒亚氨基甲酰胺转化成各种官能化的硒亚氨基甲唑酮。制备了水杨醛硒亚氨基卡巴zone及其1,2-萘基衍生物,并与某些Pd(II)和Pt(II)膦配合物反应,得到[M(L Se)(P)]类型的化合物,其中M = Pt和Pd ,L Se是双去质子化的亚硒酰胺,P是单齿膦。在这些络合物中,配体充当三齿双阴离子[Se–N–O] 2-配体,这已通过Pd衍生物的单晶X射线衍射证实。
    DOI:
    10.1016/j.jorganchem.2010.03.029
  • 作为产物:
    参考文献:
    名称:
    The Anticalcific Effect of Glutaraldehyde Detoxification on Bioprosthetic Aortic Wall Tissue in the Sheep Model
    摘要:
    Background: Increasing concentrations of glutaraldehyde (GA) lead to a decreased rather than increased calcification of bioprosthetic aortic wall tissue. This study determined to what extent the benefit of better cross-linking is masked by the intrinsic propensity of GA towards calcification. Materials and Methods: Porcine aortic roots were immediately fixed at the abattoir at three different concentrations of GA (0.2%, 1.0%, and 3.0% for 1 week at 4 C). Subsequently, roots underwent a GA extraction process using high volumes of Urazole solution (acetic acid buffer, pH 4.5, 37degreesC, 1 week) followed by NaBH4 reduction (2 days, 37 C). Roots were implanted in the distal aortic arch of young sheep for 6 weeks and 6 months. Calcium analysis was quantitatively done by atomic absorption spectrophotometry and qualitatively assessed by light microscopy on Von Kossa stains. Results: There was a distinct anticalcification effect of GA detoxification after 6 weeks (56.8% to 97.9%; 95% confidence interval [CI]), which stabilized on a more moderate level after 6 months of implantation (19.1% to 31.6%; 95% CI). The most pronounced effect of GA extraction was seen in 0.2% fixed tissue, where aortic wall calcification was mitigated by 97% and 32% after 6 weeks and 6 months, respectively. Mitigation of aortic wall calcification was 71% (6 weeks) and 21% (6 months) in the 3.0% GA group. The combined effect of higher cross-link density and detoxification achieved an 82% (6 weeks) and 48% (6 months) reduction of calcium levels in the 3.0% GA group. In long-term implants (6 months), detoxification alone on top of standard 0.2% GA fixation was as effective (from 174.1 +/- 11.9 mug/mg without detoxification to 119.3 +/- 19.3 mug/mg with detoxification) as 3.0% fixation (114.8 +/- 10.0 mug/mg without detoxification to 91.3 +/- 11.5 mug/mg with detoxification). Conclusion: We were able to determine in the circulatory sheep model to what degree the intrinsic procalcific effect of GA counteracts the protective effect of higher cross-link density. Our study also established that the effect of detoxification is particularly pronounced in commercial low-grade fixation.
    DOI:
    10.1111/j.1540-8191.2001.tb00551.x
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