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3,3-dimethyl-4-heptyloxetan-2-one | 131436-07-2

中文名称
——
中文别名
——
英文名称
3,3-dimethyl-4-heptyloxetan-2-one
英文别名
4-Heptyl-3,3-dimethyloxetan-2-one
3,3-dimethyl-4-heptyloxetan-2-one化学式
CAS
131436-07-2
化学式
C12H22O2
mdl
——
分子量
198.305
InChiKey
AFJLPKFRIOJFPH-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):
    4.2
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3,3-dimethyl-4-heptyloxetan-2-one丙烯胺三乙胺 作用下, 以 二氯甲烷 为溶剂, 以57%的产率得到3-hydroxy-2,2-dimethyl-N-prop-2-enyldecanamide
    参考文献:
    名称:
    On the antibiotic activity of oxazolomycin
    摘要:
    Structural analysis of oxazolomycin and simpler fragments containing a common 3-hydroxy-2,2-dimethylpropanamide moiety has indicated that a U-shaped conformation is preferred, in some cases stabilised by hydrogen bonding between the N-H and O-H residues, as shown by a combination of molecular modelling, NMR spectroscopic and single crystal X-ray analysis. A direct synthesis of this unit has been established via the opening of b-lactones by a range of amines, and their antibacterial activity been shown to vary with the hydrophobic character of the substituents. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.05.105
  • 作为产物:
    描述:
    正辛醛S-苯基硫代异丁酸酯正丁基锂二异丙胺 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 3.62h, 以54%的产率得到3,3-dimethyl-4-heptyloxetan-2-one
    参考文献:
    名称:
    SYNTHESIS OF b-LACTONES AND ALKENES VIA THIOL ESTERS: (E)-2,3-DIMETHYL-3-DODECENE
    摘要:
    DOI:
    10.15227/orgsyn.073.0061
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文献信息

  • A practical and efficient method for the synthesis of .beta.-lactones
    作者:Rick L. Danheiser、James S. Nowick
    DOI:10.1021/jo00003a047
    日期:1991.2
    This paper describes a convenient one-step preparation of beta-lactones based on the addition of thiol ester enolates to carbonyl compounds. Under the proper conditions the resulting aldolates undergo spontaneous cyclization to produce beta-lactones in good to excellent yield. The new beta-lactone synthesis provides access to 2-oxetanones with a variety of substituents and substitution patterns. In general, thiol ester enolates combine with carbonyl compounds to form the less sterically crowded beta-lactone diastereomers, and in some cases the reaction proceeds with excellent stereoselectivity. In conjunction with the stereospecific decarboxylation of beta-lactones, this chemistry also provides a very attractive approach to the synthesis of substituted alkenes.
  • DANHEISER, RICK L.;NOWICK, JAMES S., J. ORG. CHEM., 56,(1991) N, C. 1176-1185
    作者:DANHEISER, RICK L.、NOWICK, JAMES S.
    DOI:——
    日期:——
  • Inhibition of fatty acid synthase by beta-lactones and other compounds for inhibition of cellular proliferation
    申请人:——
    公开号:US20040024050A1
    公开(公告)日:2004-02-05
    The present invention features methods of treating a cancer in a subject by administering an effective amount of a beta-lactone to the subject. The invention also features methods of inhibiting angiogenesis in a subject by administering an effective amount of an inhibitor of fatty acid synthase to the subject. These methods can be used to treat a variety of cancers and other diseases and conditions. The invention also features methods of identifying beta-lactones and other compounds that can be used in the methods of the invention for the treatment of tumors, inhibition of angiogenesis, and the treatment of diseases and conditions that involve pathological angiogenesis.
  • [EN] INHIBITION OF FATTY ACID SYNTHASE BY BETA-LACTONES AND OTHER COMPOUNDS FOR INHIBITION OF CELLULAR PROLIFERATION<br/>[FR] INHIBITION DE SYNTHASE D'ACIDE GRAS PAR BETA-LACTONES ET PAR D'AUTRES COMPOSES DESTINES A INHIBER LA PROLIFERATION CELLULAIRE
    申请人:BURNHAM INST
    公开号:WO2003088975A1
    公开(公告)日:2003-10-30
    The present invention features methods of treating a cancer in a subject by administering an effective amount of a beta-lactone to the subject. The invention also features methods of inhibiting angiogenesis in a subject by administering an effective amount of an inhibitor of fatty acid synthase to the subject. These methods can be used to treat a variety of cancers and other diseases and conditions. The invention also features methods of identifying beta-lactones and other compounds that can be used in the methods of the invention for the treatment of tumors, inhibition of angiogenesis, and the treatment of diseases and conditions that involve pathological angiogenesis.
  • SYNTHESIS OF b-LACTONES AND ALKENES VIA THIOL ESTERS: (E)-2,3-DIMETHYL-3-DODECENE
    作者:Danheiser, Rick L.、Nowick, James S.、Lee, Janette H.、Miller, Raymond F.、Huboux, Alexandre H.、Mathre, David J.、Shinkai, Ichiro
    DOI:10.15227/orgsyn.073.0061
    日期:——
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