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2-[(2-Fluorophenoxy)methyl]-4,5-dihydro-1,3-oxazole | 1063738-02-2

中文名称
——
中文别名
——
英文名称
2-[(2-Fluorophenoxy)methyl]-4,5-dihydro-1,3-oxazole
英文别名
——
2-[(2-Fluorophenoxy)methyl]-4,5-dihydro-1,3-oxazole化学式
CAS
1063738-02-2
化学式
C10H10FNO2
mdl
——
分子量
195.193
InChiKey
OODHIQKDEIOIOH-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):
    1.6
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    30.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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

  • 作为产物:
    参考文献:
    名称:
    Synthesis and anti-inflammatory activity of 2-aryloxy methyl oxazolines
    摘要:
    A series of potential biologically active 2-aryloxy methyl oxazolines 3a-n have been synthesized from substituted hydroxybenzenes 1a-n with good chemical yield. The compounds 3a-n were screened for their anti-inflammatory, ulcerogenic, cyclooxygenase activities and also for their acute toxicity. The potency of the compounds was compared with that of the standard drugs, aspirin and phenyl butazone. The outcome indicates that compounds 3b (48.2%), 3h (48.5%) and 31 (46.5%) offered significant anti-inflammatory activity with low ulcerogenic activity than the standard drugs. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.07.029
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文献信息

  • Synthesis and anti-inflammatory activity of 2-aryloxy methyl oxazolines
    作者:Shaukath Ara Khanum、Noor Fatima Khanum、M. Shashikanth
    DOI:10.1016/j.bmcl.2008.07.029
    日期:2008.8
    A series of potential biologically active 2-aryloxy methyl oxazolines 3a-n have been synthesized from substituted hydroxybenzenes 1a-n with good chemical yield. The compounds 3a-n were screened for their anti-inflammatory, ulcerogenic, cyclooxygenase activities and also for their acute toxicity. The potency of the compounds was compared with that of the standard drugs, aspirin and phenyl butazone. The outcome indicates that compounds 3b (48.2%), 3h (48.5%) and 31 (46.5%) offered significant anti-inflammatory activity with low ulcerogenic activity than the standard drugs. (C) 2008 Elsevier Ltd. All rights reserved.
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