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6-methyl-nonan-4-one | 6175-53-7

中文名称
——
中文别名
——
英文名称
6-methyl-nonan-4-one
英文别名
6-Methyl-nonan-4-on;6-Methylnonan-4-one
6-methyl-nonan-4-one化学式
CAS
6175-53-7
化学式
C10H20O
mdl
——
分子量
156.268
InChiKey
DWPDEDNGRXAMMM-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:
    192-193 °C(Press: 715 Torr)
  • 密度:
    0.817±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    异己烯正丁醛 反应 19.0h, 生成 6-methyl-nonan-4-one
    参考文献:
    名称:
    Rabilloud,G., Bulletin de la Societe Chimique de France, 1966, p. 634 - 639
    摘要:
    DOI:
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文献信息

  • Process for producing alcohols and ketones
    申请人:SUMITOMO CHEMICAL COMPANY, LIMITED
    公开号:EP0531715A1
    公开(公告)日:1993-03-17
    The present invention provides a process for the oxidation of straight-chain, branched-chain or cyclic alkanes of 1-20 carbon atoms and benzene derivatives represented by the following formulas (1) - (2). The alcohols and ketones obtained by the oxidation of the alkanes mentioned above and those by the oxidation of the benzene derivatives mentioned above represented by the following formulas (3) - (6) are important as basic starting materials in producing various chemical products including resins, such as nylon and polyester, pharmaceuticals, agricultural chemicals, perfumes, dyes, etc.
    本发明提供了一种氧化 1-20 个碳原子的直链、支链或环状烷烃以及由下列式子 (1) - (2) 表示的苯衍生物的工艺。由上述烷烃氧化得到的醇和酮以及由下列式子(3)-(6)表示的上述苯衍生物氧化得到的醇和酮是生产各种化学产品的重要基本起始原料,包括树脂(如尼龙和聚酯)、药品、农药、香水、染料等。
  • Karrer et al., Helvetica Chimica Acta, 1930, vol. 13, p. 1300
    作者:Karrer et al.
    DOI:——
    日期:——
  • MEDICATION ADHERENCE MONITORING DEVICE
    申请人:UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC.
    公开号:US20170074857A1
    公开(公告)日:2017-03-16
    A Self Monitoring And Reporting Therapeutics, SMART® composition, method, apparatus and system are provided which flexibly provide options, by combining different embodiments of the device with different embodiments of the composition, the ability to conduct definitive medication adherence monitoring over the short term (Acute Medication Adherence Monitoring, immediately up to an hour or so after taking a medication), intermediate term (Intermediate Medication Adherence Monitoring, IMAM, an hour or so to a day or so after taking a medication), and longer term (Chronic Medication Adherence Monitoring, CMAM, a day to several days after taking a medication).
  • US5426237A
    申请人:——
    公开号:US5426237A
    公开(公告)日:1995-06-20
  • [EN] METHODS FOR PRODUCING CYCLIC AND ACYCLIC KETONES<br/>[FR] PROCÉDÉS DE PRODUCTION DE CÉTONES CYCLIQUES ET ACYCLIQUES
    申请人:UNIV CALIFORNIA
    公开号:WO2015148412A2
    公开(公告)日:2015-10-01
    Provided herein are methods for producing cyclic and acyclic ketones from trimerization and dimerization of alkyl ketones, including for example methyl ketones. Such cyclic and acyclic ketones may be suitable for use as fuel and lubricant precursors, and may be hydrodeoxygenated to form their corresponding cycloalkanes and alkanes. Such cycloalkanes and alkanes may be suitable for use as fuels, including jet fuels, and lubricants.
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