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2-(4-chlorophenyl)-2,3-dihydrobenzo[e][1,3]oxazin-4-one | 35141-49-2

中文名称
——
中文别名
——
英文名称
2-(4-chlorophenyl)-2,3-dihydrobenzo[e][1,3]oxazin-4-one
英文别名
2-(4-chloro-phenyl)-2,3-dihydro-benz[e][1,3]oxazin-4-one;2-(4-Chlor-phenyl)-2,3-dihydro-benz[e][1,3]oxazin-4-on;2-(4-Chlorophenyl)-2H-benzo[e][1,3]oxazin-4(3H)-one;2-(4-chlorophenyl)-2,3-dihydro-1,3-benzoxazin-4-one
2-(4-chlorophenyl)-2,3-dihydrobenzo[e][1,3]oxazin-4-one化学式
CAS
35141-49-2
化学式
C14H10ClNO2
mdl
——
分子量
259.692
InChiKey
FSKJCHUOYBRXMU-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

  • 溶解度:
    1.7 [ug/mL]

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    18
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    38.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis and Anticonvulsant Activity Evaluation of 2-Phenyl-2H-benzo[e][1,3]oxazin-4(3H)-ones
    作者:Li-Jing Cui、Jun Guo、Guo-Hua Gong、Zhe-Shan Quan
    DOI:10.14233/ajchem.2014.15725
    日期:——
    A series of new 2-phenyl-2H-benzo[e][1,3]oxazin-4(3H)-one derivatives (1a-1t) were designed based on the known anticonvulsant activity of quinolinone derivatives. All target compounds 1a-1t, characterized by IR, 1H NMR and MS, have been evaluated for their anticonvulsant activity against MES-induced seizures. The pharmacological results showed that all the compounds displayed some degree of anticonvulsant activity. Among them, 2-phenyl-2,3-dihydrobenzo[e][1,3]oxazin-4-one (1a) and 2-(2-fluorophenyl)-2,3-dihydrobenzo[e][1,3]oxazin-4-one (1b) were considerd more promising because of their lower ED50 (34.1 and 28.4 mg/kg) and higher protective index (11.1 and 8.0).
    基于喹啉酮衍生物已知的抗惊厥活性,设计了一系列新型2-苯基-2H-苯并[e][1,3]恶嗪-4(3H)-酮衍生物(1a-1t)。所有目标化合物 1a-1t 均通过 IR、1H NMR 和 MS 进行表征,并评估了其针对 MES 诱导的癫痫发作的抗惊厥活性。药理学结果表明所有化合物均表现出一定程度的抗惊厥活性。其中,2-苯基-2,3-二氢苯并[e][1,3]恶嗪-4-酮(1a)和2-(2-氟苯基)-2,3-二氢苯并[e][1,3] oxazin-4-one (1b) 被认为更有前景,因为其 ED50 较低(34.1 和 28.4 mg/kg),保护指数较高(11.1 和 8.0)。
  • One-Pot Heterocondensation for Benzoxazinone Derivatives Using Sodium Perborate as Catalyst
    作者:Mazaahir Kidwai、Kavita Singhal、Priya Singhal
    DOI:10.3987/com-07-11046
    日期:——
    An efficient synthesis of series of benzoxazinones, employing sodium perborate tetrahydrate (SPB) as a condensing agent is described. SPB in water and formic acid system is proved as a selective catalyst of hydration for cyanides. The rate enhancement and high yield is attributed to the coupling of suitable catalyst with this solvent system. This methodology eliminates the number of steps during the reaction.
  • KAMETANI TETSUJI; KIGASAWA KAZUO; HIIRAGI MINEHURU; WAKISAKA KIKUO; SUGI +, YAKUGAKU DZASSI, YAKUGAKU ZASSNI, J. PHARM. SOS. JAR., 1979, 99, NO 11, 1+
    作者:KAMETANI TETSUJI、 KIGASAWA KAZUO、 HIIRAGI MINEHURU、 WAKISAKA KIKUO、 SUGI +
    DOI:——
    日期:——
  • Rao, Gopal Krishna; Rajasekaran; Sanjay Pai, Indian Journal of Heterocyclic Chemistry, 2010, vol. 19, # 3, p. 293 - 294
    作者:Rao, Gopal Krishna、Rajasekaran、Sanjay Pai
    DOI:——
    日期:——
  • One Pot Synthesis of Benzopyranones and Benzoxazinones Catalyzed by MMO
    作者:Bhagi, A. K.、Singh, K. P.、Kumar, Amit、Priya、Manav, Navneet
    DOI:10.56042/ijc.v61i11.65837
    日期:——
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