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7-hydroxyhept-4-ynal | 165619-44-3

中文名称
——
中文别名
——
英文名称
7-hydroxyhept-4-ynal
英文别名
——
7-hydroxyhept-4-ynal化学式
CAS
165619-44-3
化学式
C7H10O2
mdl
——
分子量
126.155
InChiKey
JRTKSZVQQUZTTM-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):
    0
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-hydroxyhept-4-ynalsilver(l) oxide 作用下, 以 乙醇 为溶剂, 以80%的产率得到7-hydroxyhept-4-ynoic acid
    参考文献:
    名称:
    Tu, Yong Qiang; Byriel, Karl A.; Kennard, Colin H. L., Journal of the Chemical Society. Perkin transactions I, 1995, # 10, p. 1309 - 1316
    摘要:
    DOI:
  • 作为产物:
    描述:
    丙烯醛3-丁炔-1-醇 在 palladium diacetate 、 三甲基膦 作用下, 以 丙酮 为溶剂, 反应 7.0h, 以52%的产率得到7-hydroxyhept-4-ynal
    参考文献:
    名称:
    Palladium-catalyzed 1,4-addition of terminal alkynes to acrolein
    摘要:
    A Pd(OAc)(2)-PMe3 catalyzed 1,4-addition of terminal alkynes to acrolein has been developed with an environmentally conscious methodology on water. The reaction conditions were optimized to favor 1,4-addition over acrolein polymerization. The scope of the reaction was explored as well as its performance in acetone. A wide variety of 4-alkynals were obtained in moderate to good yields, thus showing the versatility of this reaction. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2015.05.087
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文献信息

  • Palladium-catalyzed 1,4-addition of terminal alkynes to acrolein
    作者:Haining Wang、Zoë Hearne、Thomas Knauber、Maria Dalko、Julien Hitce、Xavier Marat、Magali Moreau、Chao-Jun Li
    DOI:10.1016/j.tet.2015.05.087
    日期:2015.9
    A Pd(OAc)(2)-PMe3 catalyzed 1,4-addition of terminal alkynes to acrolein has been developed with an environmentally conscious methodology on water. The reaction conditions were optimized to favor 1,4-addition over acrolein polymerization. The scope of the reaction was explored as well as its performance in acetone. A wide variety of 4-alkynals were obtained in moderate to good yields, thus showing the versatility of this reaction. (C) 2015 Elsevier Ltd. All rights reserved.
  • Tu, Yong Qiang; Byriel, Karl A.; Kennard, Colin H. L., Journal of the Chemical Society. Perkin transactions I, 1995, # 10, p. 1309 - 1316
    作者:Tu, Yong Qiang、Byriel, Karl A.、Kennard, Colin H. L.、Kitching, William
    DOI:——
    日期:——
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