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4-Methyl-undec-1-en-4-ol | 72473-93-9

中文名称
——
中文别名
——
英文名称
4-Methyl-undec-1-en-4-ol
英文别名
4-Methylundec-1-en-4-ol
4-Methyl-undec-1-en-4-ol化学式
CAS
72473-93-9
化学式
C12H24O
mdl
——
分子量
184.322
InChiKey
GDLZUVHPPDXIOU-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):
    4.3
  • 重原子数:
    13
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    4-Methyl-undec-1-en-4-ol 以85%的产率得到
    参考文献:
    名称:
    INABA, TERUHIKO;SAKAMOTO, MASAMI;WATANABE, SHOJI;TAKAHASHI, IKUFUMI;FUJIT+, J. CHEM. TECHNOL. AND BIOTECHNOL., 48,(1990) N, C. 483-492
    摘要:
    DOI:
  • 作为产物:
    描述:
    十一碳-1-烯-4-酮 以95%的产率得到
    参考文献:
    名称:
    FUJITA TSUTOMU; WATANABE SHOJI; SUGA KYOICHI; INABA TERUHIKO, J. CHEM. TECHNOL. AND BIOTECHNOL., 1979, 29, NO 2, 100-106
    摘要:
    DOI:
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文献信息

  • Organomanganese (II) reagents XX: Manganese mediated Barbier and Reformatsky like reactions an efficient route to homoallylic alcohols and β-acetoxyesters
    作者:Gérard Cahiez、Pierre-Yves Chavant
    DOI:10.1016/s0040-4039(00)70700-3
    日期:1989.1
    Allylic halides and α-bromoesters react with manganese metal in ethyl acetate; THF can also be used as solvent if a catalytic amount of zinc chloride is added to the reaction mixture. When the reaction is performed in the presence of various aldehydes or ketones, excellent yields of 1,2-addition products are obtained in preparative conditions.
    烯丙基卤化物和α-溴酸酯与锰金属在乙酸乙酯中反应;如果将催化量的氯化锌加入到反应混合物中,则THF也可以用作溶剂。当反应在各种醛或酮的存在下进行时,在制备条件下可获得极好的1,2-加成产物收率。
  • 1,8-Bis(allylstannyl)naphthalene Derivatives as Neutral Allylation Agents: Rate Acceleration by Chelation-Induced Lewis Acidity
    作者:Naoki Asao、Pingli Liu、Keiji Maruoka
    DOI:10.1002/anie.199725071
    日期:1997.12.1
  • Allylation of ketones with allylstannanes catalyzed by Lewis acid–Lewis base combined reagents
    作者:Ryo Hamasaki、Yukiyasu Chounan、Hiroshi Horino、Yoshinori Yamamoto
    DOI:10.1016/s0040-4039(00)01755-x
    日期:2000.12
    Although the Lewis acid promoted allylation of ketones with allylstannanes gives the corresponding tert-homoallyl alcohols in lower yields in comparison with those of aldehydes, the use of Lewis acid-Lewis base combined catalysts such as Zn(OTf)(2)-2,6-lutidine and Zn(OTf)(2)-pyridine dramatically enhances the yield of the tert-alcohols. (C) 2000 Published by Elsevier Science Ltd.
  • CAHIEZ, G.;CHAVANT, P. -Y., TETRAHEDRON LETT., 30,(1989) N2, C. 7373-7376
    作者:CAHIEZ, G.、CHAVANT, P. -Y.
    DOI:——
    日期:——
  • INABA, TERUHIKO;SAKAMOTO, MASAMI;WATANABE, SHOJI;TAKAHASHI, IKUFUMI;FUJIT+, J. CHEM. TECHNOL. AND BIOTECHNOL., 48,(1990) N, C. 483-492
    作者:INABA, TERUHIKO、SAKAMOTO, MASAMI、WATANABE, SHOJI、TAKAHASHI, IKUFUMI、FUJIT+
    DOI:——
    日期:——
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