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1-(4-tert-butyl-2-methyl-phenyl)-ethanone | 132777-92-5

中文名称
——
中文别名
——
英文名称
1-(4-tert-butyl-2-methyl-phenyl)-ethanone
英文别名
1-(4-tert-Butyl-2-methyl-phenyl)-aethanon;21-Oxo-1-methyl-2-aethyl-5-tert.-butyl-benzol;Methyl-(2-methyl-4-tert.-butyl-phenyl)-keton;2-Methyl-4-tert.-butyl-acetophenon;5-tert.-Butyl-2-acetyl-toluol;1-(4-Tert-butyl-2-methylphenyl)ethanone
1-(4-<i>tert</i>-butyl-2-methyl-phenyl)-ethanone化学式
CAS
132777-92-5
化学式
C13H18O
mdl
——
分子量
190.285
InChiKey
CHQZPHMFRMBUTA-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:
    90 °C(Press: 1 Torr)
  • 密度:
    0.9627 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.6
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

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

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文献信息

  • Electrochemically promoted Friedel–Crafts acylation of aromatic compounds
    作者:G. Karthik、K. Kulangiappar、Frank Marken、M. Anbu Kulandainathan
    DOI:10.1016/j.tetlet.2008.02.084
    日期:2008.4
    Friedel–Crafts acylation is carried out with several aromatic substrates in the presence of an electrochemically active aluminium anode to minimize the inorganic reagents. Only a catalytic amount of AlCl3 (5 mol %) is required to enable the anodic polarization of the aluminium electrode to promote continuous acylation. This process typically gave products in good yields (70–96%).
    Friedel-Crafts酰化反应是在电化学活性铝阳极存在下,用几种芳香族底物进行的,以最大程度地减少无机试剂。仅需要催化量的AlCl 3(5mol%)以使铝电极的阳极极化能够促进连续的酰化。此过程通常使产品具有良好的收率(70-96%)。
  • 10A-AZALIDE COMPOUND CROSSLINKED AT 10A- AND 12-POSITIONS
    申请人:Sugimoto Tomohiro
    公开号:US20110237784A1
    公开(公告)日:2011-09-29
    A novel 10a-azalide compound crosslinked at the 10a- and 12-positions, which is represented by the following formula, and is effective on even Hemophilus influenzae , or erythromycin resistant bacteria (e.g., resistant pneumococci and streptococci).
    一种新型的10a-azalide化合物,其在10a-和12-位置交联,化学式如下,并且对于Hemophilus influenzae,或者对红霉素产生耐药性的细菌(例如耐药性肺炎球菌和链球菌)具有有效性。
  • α-Methylation at benzylic fragment of N-aryl-N′-benzyl ureas provides TRPV1 antagonists with better pharmacokinetic properties and higher efficacy in inflammatory pain model
    作者:Arthur Gomtsyan、Erol K. Bayburt、Ryan Keddy、Sean C. Turner、Tammie K. Jinkerson、Stanley Didomenico、Richard J. Perner、John R. Koenig、Irene Drizin、Heath A. McDonald、Carol S. Surowy、Prisca Honore、Joe Mikusa、Kennan C. Marsh、Jill M. Wetter、Connie R. Faltynek、Chih-Hung Lee
    DOI:10.1016/j.bmcl.2007.04.105
    日期:2007.7
    SAR studies for N-aryl-N '-benzyl urea class of TRPV1 antagonists have been extended to cover alpha-benzyl alkylation. Alkylated compounds showed weaker in vitro potencies in blocking capsaicin activation of TRPV1 receptor, but possessed improved pharmacokinetic properties. Further structural manipulations that included replacement of isoquinoline core with indazole and isolation of single enantiomer led to TRPV1 antagonists like (R)-16a with superior pharmacokinetic properties and greater potency in animal model of inflammatory pain. (C) 2007 Elsevier Ltd. All rights reserved.
  • Isomerization Accompanying the Acetylation of p-t-Butyltoluene
    作者:W. J. HEINTZELMAN、B. B. CORSON
    DOI:10.1021/jo01352a004
    日期:1957.1
  • Baur-Thurgau, Chemische Berichte, 1900, vol. 33, p. 2568
    作者:Baur-Thurgau
    DOI:——
    日期:——
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