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3-(呋喃-2-甲基)-7,7-二甲基-7,8-二氢-2H-色烯-2,5(6H)-二酮 | 1038998-64-9

中文名称
3-(呋喃-2-甲基)-7,7-二甲基-7,8-二氢-2H-色烯-2,5(6H)-二酮
中文别名
——
英文名称
3-(furan-2-ylmethyl)-7,7-dimethyl-7,8-dihydro-6H-chromene-2,5-dione
英文别名
3-(furan-2-ylmethyl)-7,7-dimethyl-7,8-dihydro-2H-chromene-2,5(6H)-dione;3-(furan-2-ylmethyl)-7,7-dimethyl-6,8-dihydrochromene-2,5-dione
3-(呋喃-2-甲基)-7,7-二甲基-7,8-二氢-2H-色烯-2,5(6H)-二酮化学式
CAS
1038998-64-9
化学式
C16H16O4
mdl
——
分子量
272.301
InChiKey
XIUUXILNVPNIOV-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

  • 沸点:
    435.1±45.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    20
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    56.5
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • An Efficient Synthesis of 2-Hydroxy-7,8-dihydroquinolin-5(6<i>H</i>)-ones and 7,8-Dihydroquinoline-2,5(1<i>H</i>,6<i>H</i>)-diones from Morita-Baylis-Hillman Adduct Acetates
    作者:Weike Su、Weihui Zhong、Fuliang Lin、Ren’er Chen
    DOI:10.1055/s-2008-1078601
    日期:2008.8
    A series of 2-hydroxy-7,8-dihydroquinolin-5(6 H)-ones and7,8-dihydroquinoline-2,5(1 H,6 H)-diones have been synthesized in goodto excellent yields from Morita-Baylis-Hillman -adductacetates, cyclohexane-1,3-diones and ammonium acetate or primaryamines in one pot under solvent-free conditions.
    Morita-Baylis-合成了一系列 2-hydroxy-7,8-dihydroquinolin-5(6 H)-ones 和 7,8-dihydroquinoline-2,5(1 H,6 H)-diones-在无溶剂条件下,Hillman - 乙酸加合物、环己烷-1,3-二酮和乙酸铵或伯胺在一锅中。
  • An efficient synthesis of 3-arylmethyl-7,8-dihydro-6H-chromene-2,5-diones from Baylis–Hillman adduct acetates under solvent-free conditions
    作者:Weihui Zhong、Yongzhi Zhao、Weike Su
    DOI:10.1016/j.tet.2008.04.003
    日期:2008.6
    A simple, efficient synthesis of 3-arylmethyl-7,8-dihydro-6H-chromene-2,5-dione 4 from Baylis-Hillman adduct acetates derived from aromatic aldehydes and cyclohexane-1,3-diones under solvent-free conditions is described. Interestingly, when Baylis-Hillman adducts derived from aliphatic aldehydes were tested under the similar conditions, the unexpected stereoisomers 5 and 6 were obtained in moderate yields. A plausible mechanism for the formation of 4-6 is proposed. (C) 2008 Elsevier Ltd. All rights reserved.
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