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tert-butyl (10-phenyl-9-anthryl)nitroxide

中文名称
——
中文别名
——
英文名称
tert-butyl (10-phenyl-9-anthryl)nitroxide
英文别名
BPAN
tert-butyl (10-phenyl-9-anthryl)nitroxide化学式
CAS
——
化学式
C24H24NO
mdl
——
分子量
342.461
InChiKey
QLBNLZZXDDEGOO-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):
    6.7
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    4.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    tert-butyl (10-phenyl-9-anthryl)nitroxideVitamin C 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以96%的产率得到N-tert-butyl N-(10-phenyl-9-anthryl) hydroxylamine
    参考文献:
    名称:
    Scavenging and Characterization of Short-Lived Radicals Using a Novel Stable Nitroxide Radical with a Characteristic UV–vis Absorption Spectrum
    摘要:
    A stable tert-butyl(10-phenyl-9-anthryl)nitroxide (BPAN) radical was newly synthesized and used for the capture/characterization of reactive radicals. Adducts obtained from the reactions of BPAN with in situ generated reactive radicals showed excellent stability, assuring complete isolation and purification. The structures of the adducts were established by LC-MS and NMR analyses.
    DOI:
    10.1021/ol501328k
  • 作为产物:
    描述:
    参考文献:
    名称:
    Scavenging and Characterization of Short-Lived Radicals Using a Novel Stable Nitroxide Radical with a Characteristic UV–vis Absorption Spectrum
    摘要:
    A stable tert-butyl(10-phenyl-9-anthryl)nitroxide (BPAN) radical was newly synthesized and used for the capture/characterization of reactive radicals. Adducts obtained from the reactions of BPAN with in situ generated reactive radicals showed excellent stability, assuring complete isolation and purification. The structures of the adducts were established by LC-MS and NMR analyses.
    DOI:
    10.1021/ol501328k
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文献信息

  • Scavenging and Characterization of Short-Lived Radicals Using a Novel Stable Nitroxide Radical with a Characteristic UV–vis Absorption Spectrum
    作者:Ryuta Toba、Hiroaki Gotoh、Kazuhisa Sakakibara
    DOI:10.1021/ol501328k
    日期:2014.8.1
    A stable tert-butyl(10-phenyl-9-anthryl)nitroxide (BPAN) radical was newly synthesized and used for the capture/characterization of reactive radicals. Adducts obtained from the reactions of BPAN with in situ generated reactive radicals showed excellent stability, assuring complete isolation and purification. The structures of the adducts were established by LC-MS and NMR analyses.
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同类化合物

金不换萘酚 金不换素 蒽,9,10-二[4-(2,2-二苯基乙烯基)苯基]- 萘并[2,3-c]呋喃-1,3-二酮,6-甲氧基-4-(4-甲氧苯基)- 萘并[2,3-c]呋喃-1(3H)-酮,7-羟基-4-(3-甲氧苯基)- 萘并[2,3-c]呋喃-1(3H)-酮,4-(2-氟苯基)-7-(苯基甲氧基)- 苯氧基-9苯基-10蒽 苯基-(10-苯基蒽-9-基)甲酮 红荧烯 甲基7-苯基二苯并(A,J)蒽-14-羧酸酯 甲基10-苯基-9-蒽羧酸酯 爵床脂素 B 爵床脂素 A 木酚素J1(P) 昔土米霉素 新爵床素 B 拒食胺 大麻酰胺 地蒽酚10,10'-二聚体 四去氢鬼臼毒素 叶下珠醇抑制剂A 二甲基4-(3,4-二甲氧苯基)-1-羟基-5,6,7-三甲氧基萘-2,3-二甲酸基酯 二叶草素 [4-(3,10-二羟基蒽-9-基)苯基]乙酸乙酸酯 [4-(10-羟基蒽-9-基)苯基]乙酸乙酸酯 [2-甲氧基-10-(4-甲氧基苯基)蒽-9-基]乙酸酯 [10-羟基-5-(10-羟基-7,9-二甲氧基-3-甲基-3,4-二氢-1H-苯并[g]异苯并吡喃-5-基)-7,9-二甲氧基-3-甲基-3,4-二氢-1H-苯并[g]异苯并吡喃-4-基]乙酸酯 [10-(9,9-二甲基芴-2-基)蒽-9-基]硼酸 [10-(4-叔丁基苯基)蒽-9-基]硼酸 B-[10-(4-苯基-1-萘基)-9-蒽基]硼酸 B-(9,10-二苯基-2-蒽)硼酸 9.10-二(3',5'-二羧基苯基)蒽 9-萘-1-基-10-(4-苯基苯基)蒽 9-苯基蒽 9-苯基-10-苯乙炔基菲 9-苯基-10-硝基蒽 9-苯基-10-(苯基乙炔基)蒽 9-苯基-10-(4-三苯胺)蒽 9-苯基-1,2,3,4-四氢蒽 9-羟基-10-甲氧基-5-(3,4,5-三甲氧基苯基)-8H-[2]苯并呋喃并[6,5-f][1,3]苯并二氧戊环-6-酮 9-碘-10-(10-碘蒽-9-基)蒽 9-甲氧基-10-苯基蒽 9-甲基-10-苯基菲 9-溴-10-苯基蒽 9-溴-10-[4-(2-萘基)苯基]蒽 9-溴-10-[3-(2-萘基)苯基]蒽 9-溴-10-[3-(10-溴蒽-9-基)-5-甲基苯基]蒽 9-溴-10-[1,1':3',1''-三联苯]-5'-基蒽 9-溴-10-(4-苯基萘-1-基)蒽 9-溴-10-(2-萘基)蒽