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3-bromo-valeric acid ethyl ester | 854879-55-3

中文名称
——
中文别名
——
英文名称
3-bromo-valeric acid ethyl ester
英文别名
3-Brom-valeriansaeure-aethylester;Ethyl 3-bromopentanoate
3-bromo-valeric acid ethyl ester化学式
CAS
854879-55-3
化学式
C7H13BrO2
mdl
——
分子量
209.083
InChiKey
VOEAEELHRMARKD-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):
    2.1
  • 重原子数:
    10
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3-bromo-valeric acid ethyl ester间苯三酚 、 sodium nitrite 作用下, 以 正戊烷 为溶剂, 生成 3-Nitro-valeriansaeure-aethylester
    参考文献:
    名称:
    Biernacki,W.; Urbanski,T., Bulletin de l'Academie Polonaise des Sciences, Serie des Sciences Chimiques, 1965, vol. 13, p. 349 - 354
    摘要:
    DOI:
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 氯仿五溴化磷 作用下, 生成 3-bromo-valeric acid ethyl ester
    参考文献:
    名称:
    Levene; Mori, Journal of Biological Chemistry, 1928, vol. 78, p. 6
    摘要:
    DOI:
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文献信息

  • Benzopyran derivative and antiallergic agent
    申请人:Dainippon Ink and Chemicals, Inc.
    公开号:US20030096860A1
    公开(公告)日:2003-05-22
    The present invention provides a compound which is highly safe in terms of toxicity and has a stronger antiallergic action, and particularly has an action of inhibiting both immediate and delayed type allergic reactions. A benzopyran derivative represented by the general formula (I): 1 wherein R 1 is an alkyl group having 1-10 carbon atoms or an alkenyl group having 2-10 carbon atoms, and one of R 2 , R 3 , R 4 , and R 5 is an alkoxy group substituted with a hydroxy group or an alkoxy group substituted with a carboxy group, and the others are hydrogen atoms or physiologically acceptable salts thereof are superior as the active ingredient of an antiallergic agent.
    本发明提供了一种化合物,该化合物在毒性方面非常安全,并具有更强的抗过敏作用,特别是具有抑制即刻型和迟发型过敏反应的作用。一种由通式(I)表示的苯并吡喃衍生物:其中R1是具有1-10个碳原子的烷基或具有2-10个碳原子的烯基,而R2、R3、R4和R5中的一个是被羟基取代的烷氧基或被羧基取代的烷氧基,而其余的是氢原子,或其生理上可接受的盐作为抗过敏药物的活性成分。
  • Quinoline derivatives as antagonists of leukotriene D4, compositions containing the same and processes for their preparation
    申请人:RHONE-POULENC RORER INTERNATIONAL (HOLDINGS) INC.
    公开号:EP0348155A1
    公开(公告)日:1989-12-27
    This invention relates to quinolinyl compounds of the general formula: and the use of these compounds as pharmacological agents which are lipoxygenase inhibitors and/or leukotriene antagonists possessing anti-inflammatory and anti-allergic properties and their pharmaceutical compositions and processes for this preparation.
    本发明涉及通式如下的喹啉基化合物: 以及将这些化合物用作具有抗炎和抗过敏特性的脂氧合酶抑制剂和/或白三烯拮抗剂的药剂及其药物组合物和制备工艺。
  • Quinoline derivatives as antagonists of leukotriene d4, compositions containing the same and processes for their preparation
    申请人:Aventis Holdings Inc.
    公开号:EP0784052B1
    公开(公告)日:2004-09-01
  • Benzopyran derivatives and antiallergic agent containing the same
    申请人:DAINIPPON INK AND CHEMICALS, INC.
    公开号:EP1273578B1
    公开(公告)日:2005-02-23
  • US4918081A
    申请人:——
    公开号:US4918081A
    公开(公告)日:1990-04-17
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