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2-methylphenol

中文名称
——
中文别名
——
英文名称
2-methylphenol
英文别名
2-Methylcyclohexa-2,5-dien-1-ol
2-methylphenol化学式
CAS
——
化学式
C7H10O
mdl
——
分子量
110.156
InChiKey
KOUDVLIKNJAVCZ-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):
    1
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 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:
    2-methylphenol氧气 作用下, 以 1,4-二氧六环 为溶剂, 反应 6.0h, 生成 甲基苯醌
    参考文献:
    名称:
    Activated Zeolites and Heteropolyacids: An Efficient Catalysts for the Synthesis of Triacetoxyaromatic Precursors of Hydroxyquinones
    摘要:
    泰尔-温特反应在合成氢醌的前驱体三乙酸芳香化合物方面具有重要意义。氯磺酸等液态酸和杂多酸等固态酸作为高效催化剂,可以在室温下不使用有机溶剂的条件下,有效替代硫酸在醌类乙酰氧基化反应中的作用。
    DOI:
    10.14233/ajchem.2013.14276
  • 作为产物:
    描述:
    邻甲酚 在 sodium persulfate 、 sodium hydroxide 作用下, 反应 24.0h, 生成 2-methylphenol
    参考文献:
    名称:
    Activated Zeolites and Heteropolyacids: An Efficient Catalysts for the Synthesis of Triacetoxyaromatic Precursors of Hydroxyquinones
    摘要:
    泰尔-温特反应在合成氢醌的前驱体三乙酸芳香化合物方面具有重要意义。氯磺酸等液态酸和杂多酸等固态酸作为高效催化剂,可以在室温下不使用有机溶剂的条件下,有效替代硫酸在醌类乙酰氧基化反应中的作用。
    DOI:
    10.14233/ajchem.2013.14276
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文献信息

  • Probe compound for detecting and isolating enzymes and means and methods using the same
    申请人:Helmholtz-Zentrum für Infektionsforschung GmbH
    公开号:EP2230312A1
    公开(公告)日:2010-09-22
    The present invention relates to a probe compound that can comprise any substrate or metabolite of an enzymatic reaction in addition to an indicator component, such as, for example, a fluorescence dye, or the like. Moreover, the present invention relates to means for detecting enzymes in form of an array, which comprises any number of probe compounds of the invention which each comprise a different metabolite of interconnected metabolites representing the central pathways in all forms of life. Moreover, the present invention relates to a method for detecting enzymes involving the application of cell extracts or the like to the array of the invention which leads to reproducible enzymatic reactions with the substrates. These specific enzymatic reactions trigger the indicator (e.g. a fluorescence signal) and bind the enzymes to the respective cognate substrates. Moreover, the invention relates to means for isolating enzymes in form of nanoparticles coated with the probe compound of the invention. The immobilisation of the cognate substrates or metabolites on the surface of nanoparticles by means of the probe compounds allows capturing and isolating the respective enzyme, e.g. for subsequent sequencing.
    本发明涉及一种探针化合物,它可以包括酶反应的任何底物或代谢物,此外还包括指示成分,例如荧光染料或类似物。此外,本发明还涉及以阵列形式检测酶的方法,该阵列由任意数量的本发明探针化合物组成,每种探针化合物由代表所有生命形式中中心途径的相互关联的代谢物中的不同代谢物组成。此外,本发明还涉及一种检测酶的方法,该方法涉及将细胞提取物或类似物应用于本发明的阵列,从而导致与底物发生可重复的酶反应。这些特定的酶反应会触发指示剂(如荧光信号),并将酶与各自的同源底物结合。此外,本发明还涉及以涂覆有本发明探针化合物的纳米颗粒形式分离酶的方法。通过探针化合物将同源底物或代谢物固定在纳米颗粒表面,可以捕获和分离相应的酶,例如用于后续测序。
  • Modulation of Pathogenicity
    申请人:Ammendola Aldo
    公开号:US20070093534A1
    公开(公告)日:2007-04-26
    The present invention relates to the use of compounds of the general Formula (XIII): wherein A 7 is C═O, C═S, SO 2 , CH—OR 13 , C═NR 12 , or CH 2 —CHOR 13 ; A 8 is C(R 14 ) 2 , O, S, or NR 12 ; A 9 is C═O, C═S, SO 2 , CH—OR 13 , C═NR 12 , or CH 2 —CHOR 13 ; m is 0, or 1 q is 0, or 1 r is 0, or 1 R 12 is H, CH 3 , CH 2 —CH 3 , C 6 H 5 , OCH 3 , OCH 2 —CH 3 , OH, or SH; R 13 is H, CH 3 , or CH 2 —CH 3 ; R 14 is H, alkyl, alkoxy, OH, or SH;
  • Modulation of pathogcnicity
    申请人:Ammendola Aldo
    公开号:US20080194588A1
    公开(公告)日:2008-08-14
    The present invention relates to the use of compounds of the general Formula (I): wherein in Formula (I), R is H, alkyl, cycloalkyl, aryl or heteroaryl; R 1 is H, alkyl, cycloalkyl, aryl or heteroaryl; R 2 is H, alkyl, cycloalkyl, aryl or heteroaryl; A 1 and A 2 each independently represent an optionally substituted C 1 -C 20 -alkyl group which may contain one or more group(s) Z, or a monocyclic or polycyclic optionally substituted aromatic or non-aromatic ring system which may contain one or more group(s) X, and in case of a polycyclic ring system, said system contains at least one aromatic ring; Z is selected from the group consisting of S, O, N, NR 4 , CO, CO 2 , CS, SO or SO 2 X is selected from the group consisting of S, O, N, NR 4 , SO or SO 2 ;
  • Modulation of pathogenicity
    申请人:Ammendola Aldo
    公开号:US20080176938A1
    公开(公告)日:2008-07-24
    The present invention relates to the use of compounds of the general Formula (1): wherein in Formula (1), R is H, alkyl, cycloalkyl, aryl or heteroaryl; R 1 is H, alkyl, cycloalkyl, aryl or heteroaryl; R 2 is H, alkyl, cycloalkyl, aryl or heteroaryl; A 1 and A 2 each independently represent an optionally substituted C 1 -C 20 -alkyl group which may contain one or more group(s) Z, or a monocyclic or polycyclic optionally substituted aromatic or non-aromatic ring system which may contain one or more group(s) X, and in case of a polycyclic ring system, said system contains at least one aromatic ring; Z is selected from the group consisting of S, O, N, NR 4 , CO, CO 2 , CS, SO or SO 2 X is selected from the group consisting of S, O, N, NR 4 , SO or SO 2 .
  • US7335779B2
    申请人:——
    公开号:US7335779B2
    公开(公告)日:2008-02-26
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