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(Z)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3R,4S,5S,6R)-3,5-dihydroxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester | 116215-49-7

中文名称
——
中文别名
——
英文名称
(Z)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3R,4S,5S,6R)-3,5-dihydroxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester
英文别名
methyl 3,6-di-O-(4-methoxycinnamoyl)-α-D-mannopyranoside
(Z)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3R,4S,5S,6R)-3,5-dihydroxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester化学式
CAS
116215-49-7;128796-87-2
化学式
C27H30O10
mdl
——
分子量
514.529
InChiKey
LUBPPWQPHJNUPC-PRZGGUPBSA-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):
    1.98
  • 重原子数:
    37.0
  • 可旋转键数:
    10.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    129.98
  • 氢给体数:
    2.0
  • 氢受体数:
    10.0

上下游信息

  • 上游原料
    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:
    (Z)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3R,4S,5S,6R)-3,5-dihydroxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester乙酸酐4-二甲氨基吡啶 吡啶 作用下, 生成 (E)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3S,4S,5R,6R)-3,5-diacetoxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester
    参考文献:
    名称:
    Oligosaccharide microanalysis by C.D. spectroscopy. Reference curves for d-mannose derivatives
    摘要:
    This study completes the spectroscopic basis for a novel oligosaccharide microanalytical method, wherein a derivatization sequence provides monosaccharide subunits bearing two types of exciton-coupling chromophore groups ("bichromophoric") for circular dichroic spectroscopy, namely 4-bromobenzoate (lambda max 245 nm) and 4-methoxycinnamate (lambda max 311 nm). The 24 possible derivatives of methyl alpha-D-mannopyranoside bearing two chromophore and two acetate groups have been prepared and their c.d. spectra recorded. These spectra have been used to calculate the c.d. curves of the 14 possible tetrachromophic derivatives according to the pairwise additivity rule. The accuracy of these calculations has been demonstrated for six representative derivatives. The c.d. curves obtained here, together with curves of the corresponding D-glucose and D-galactose derivatives, comprise a set of 42 unique and distinctive spectra which can be utilized to identify sugars and their linkage patterns, and thus represent the basis for an alternative to methylation analysis which does not rely upon synthetic standards.
    DOI:
    10.1016/0008-6215(90)84126-f
  • 作为产物:
    描述:
    (2E)-3-(4-甲氧基苯基)丙烯酰氯甲基-D-丙噻4-二甲氨基吡啶 吡啶 作用下, 以47%的产率得到(Z)-3-(4-Methoxy-phenyl)-acrylic acid (2S,3R,4S,5S,6R)-3,5-dihydroxy-2-methoxy-6-[(E)-3-(4-methoxy-phenyl)-acryloyloxymethyl]-tetrahydro-pyran-4-yl ester
    参考文献:
    名称:
    Oligosaccharide microanalysis by C.D. spectroscopy. Reference curves for d-mannose derivatives
    摘要:
    This study completes the spectroscopic basis for a novel oligosaccharide microanalytical method, wherein a derivatization sequence provides monosaccharide subunits bearing two types of exciton-coupling chromophore groups ("bichromophoric") for circular dichroic spectroscopy, namely 4-bromobenzoate (lambda max 245 nm) and 4-methoxycinnamate (lambda max 311 nm). The 24 possible derivatives of methyl alpha-D-mannopyranoside bearing two chromophore and two acetate groups have been prepared and their c.d. spectra recorded. These spectra have been used to calculate the c.d. curves of the 14 possible tetrachromophic derivatives according to the pairwise additivity rule. The accuracy of these calculations has been demonstrated for six representative derivatives. The c.d. curves obtained here, together with curves of the corresponding D-glucose and D-galactose derivatives, comprise a set of 42 unique and distinctive spectra which can be utilized to identify sugars and their linkage patterns, and thus represent the basis for an alternative to methylation analysis which does not rely upon synthetic standards.
    DOI:
    10.1016/0008-6215(90)84126-f
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