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1-methoxy-5-methyl-2-(1'-pentanoyl)benzene

中文名称
——
中文别名
——
英文名称
1-methoxy-5-methyl-2-(1'-pentanoyl)benzene
英文别名
1-(2-Methoxy-4-methylphenyl)pentan-1-one
1-methoxy-5-methyl-2-(1'-pentanoyl)benzene化学式
CAS
——
化学式
C13H18O2
mdl
——
分子量
206.285
InChiKey
GIGXOYAATFONDX-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):
    3.3
  • 重原子数:
    15
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of E-3-Hydroxymethyl-1-methoxy-4-(1′-pentenyl)benzene
    摘要:
    The title compound with exclusively the E-geometry has been synthesized by two independent routes. When this compound was reacted with cerium(IV) ammonium nitrate, it was found that oxidative cyclisation to the corresponding 4-hydroxybenzopyrans did not occur. This further defines the structural parameters required for such oxidative cyclisations.
    DOI:
    10.1080/00397919508011471
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文献信息

  • AMINO ACID HAVING FUNCTIONAL GROUP CAPABLE OF INTERMOLECULAR HYDROGEN BONDING, PEPTIDE COMPOUND CONTAINING SAME AND METHOD FOR PRODUCTION THEREOF
    申请人:CHUGAI SEIYAKU KABUSHIKI KAISHA
    公开号:EP3896056A1
    公开(公告)日:2021-10-20
    It has been found that the membrane permeability of peptide compounds can be improved by making at least one of amino acids constituting the peptide compound be an amino acid having a side chain capable of forming an intramolecular hydrogen bond.
    研究发现,通过使构成多肽化合物的氨基酸中至少有一个氨基酸具有能够形成分子内氢键的侧链,可以改善多肽化合物的膜渗透性。
  • Synthesis of E-3-Hydroxymethyl-1-methoxy-4-(1′-pentenyl)benzene
    作者:Robin G.F. Giles、Ivan R. Green、J. Alexandre X. Pestana
    DOI:10.1080/00397919508011471
    日期:1995.12
    The title compound with exclusively the E-geometry has been synthesized by two independent routes. When this compound was reacted with cerium(IV) ammonium nitrate, it was found that oxidative cyclisation to the corresponding 4-hydroxybenzopyrans did not occur. This further defines the structural parameters required for such oxidative cyclisations.
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