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3,6-dihydro-4-methyl-2H-pyran-2-carboxylic acid | 19353-25-4

中文名称
——
中文别名
——
英文名称
3,6-dihydro-4-methyl-2H-pyran-2-carboxylic acid
英文别名
4-methyl-3,6-dihydro-2H-pyran-2-carboxylic acid;4-methyl-3,6-dihydro-2H-pyran-2-carboxylic acid
3,6-dihydro-4-methyl-2H-pyran-2-carboxylic acid化学式
CAS
19353-25-4
化学式
C7H10O3
mdl
MFCD19228487
分子量
142.155
InChiKey
RNESUVFBQQXRIC-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:
    275.6±40.0 °C(Predicted)
  • 密度:
    1.174±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.571
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    参考文献:
    名称:
    Structure Elucidation, Enantioselective Analysis, and Biogenesis of Nerol Oxide in Pelargonium Species
    摘要:
    A novel enantioselective synthesis of nerol oxide (3,6-dihydro-4-methyl-2-(2-methyl-1-propenyl)-2H-pyran) was used for the determination of the absolute configuration at C-2. The order of elution of the enantiomers on octakis-(2,3-di-O-butyryl-6-O-tert-butyldimethylsilyl)-gamma-cyclodextrin in OV 1701-vi as the chiral stationary phase in enantioselective GC was determined as (2R) before (2S). Enantioselective multidimensional GC/MS (enantio-MDGC/MS) was used for the determination of the enantiomeric ratios of nerol oxide in different geranium oils. As a result, in all investigated oils nerol oxide occurs as a racemate. The biogenesis of nerol oxide in Pelargonium species was investigated by feeding experiments using deuterium-labeled neryl glucoside as the precursor. The Pelargonium plants were able to convert the fed precursor into racemic nerol oxide, which has to be considered as a "natural racemate"
    DOI:
    10.1021/jf981245m
  • 作为产物:
    参考文献:
    名称:
    Structure Elucidation, Enantioselective Analysis, and Biogenesis of Nerol Oxide in Pelargonium Species
    摘要:
    A novel enantioselective synthesis of nerol oxide (3,6-dihydro-4-methyl-2-(2-methyl-1-propenyl)-2H-pyran) was used for the determination of the absolute configuration at C-2. The order of elution of the enantiomers on octakis-(2,3-di-O-butyryl-6-O-tert-butyldimethylsilyl)-gamma-cyclodextrin in OV 1701-vi as the chiral stationary phase in enantioselective GC was determined as (2R) before (2S). Enantioselective multidimensional GC/MS (enantio-MDGC/MS) was used for the determination of the enantiomeric ratios of nerol oxide in different geranium oils. As a result, in all investigated oils nerol oxide occurs as a racemate. The biogenesis of nerol oxide in Pelargonium species was investigated by feeding experiments using deuterium-labeled neryl glucoside as the precursor. The Pelargonium plants were able to convert the fed precursor into racemic nerol oxide, which has to be considered as a "natural racemate"
    DOI:
    10.1021/jf981245m
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文献信息

  • Merging Photoredox and Nickel Catalysis: Decarboxylative Cross-Coupling of Carboxylic Acids with Vinyl Halides
    作者:Adam Noble、Stefan J. McCarver、David W. C. MacMillan
    DOI:10.1021/ja511913h
    日期:2015.1.21
    Decarboxylative cross-coupling of alkyl carboxylic acids with vinyl halides has been accomplished through the synergistic merger of photoredox and nickel catalysis. This new methodology has been successfully applied to a variety of α-oxy and α-amino acids, as well as simple hydrocarbon-substituted acids. Diverse vinyl iodides and bromides give rise to vinylation products in high efficiency under mild
    烷基羧酸乙烯基卤化物的脱羧交叉偶联是通过光氧化还原和催化的协同合并实现的。这种新方法已成功应用于各种α-氧基和α-氨基酸,以及简单的烃取代酸。不同的乙烯基化物和化物在温和、操作简单的反应条件下高效地产生乙烯基化产物。
  • Enhancement of Dienophilic and Enophilic Reactivity of the Glyoxylic Acid by Bismuth(III) Triflate in the Presence of Water
    作者:H. Laurent-Robert、C. Le Roux、J. Dubac
    DOI:10.1055/s-1998-1869
    日期:1998.10
    Bismuth(III) trifluoromethanesulfonate (1) is found to efficiently catalyze carbonyl-Diels-Alder or carbonyl-ene reactions between glyoxylic acid and classical dienes or substituted olefins, in the presence of water.
    甲烷磺酸(III)(1)在的存在下,能够高效催化羟基乙酸与经典二烯或取代烯烃之间的羰基-达尔斯-阿尔德反应或羰基-烯反应。
  • Aqueous hetero Diels-Alder reactions: The carbonyl case.
    作者:A. Lubineau、J. Augé、E. Grand、N. Lubin
    DOI:10.1016/s0040-4020(01)81759-2
    日期:1994.8
    Commercially available aqueous solution of glyoxylic acid, pyruvaldehyde and glyoxal were shown to react with cyclic or non-cyclic dienes to give the corresponding cycloadducts and/or alpha-hydroxy gamma-lactones. Activated ketone (Pyruvic acid) was shown to react as well in the same conditions.
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