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1,1,1-三氟-3-甲基己烷-2,4-二酮 | 392-48-3

中文名称
1,1,1-三氟-3-甲基己烷-2,4-二酮
中文别名
——
英文名称
1,1,1-trifluoro-3-methyl-2,4-hexanedione
英文别名
1,1,1-trifluoro-3-methyl-hexane-2,4-dione;1,1,1-Trifluor-3-methyl-hexan-2,4-dion;1,1,1-Trifluoro-3-methylhexane-2,4-dione
1,1,1-三氟-3-甲基己烷-2,4-二酮化学式
CAS
392-48-3
化学式
C7H9F3O2
mdl
——
分子量
182.142
InChiKey
IRBFWXBYIVISFR-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:
    74 °C(Press: 43 Torr)
  • 密度:
    1.22 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 海关编码:
    2914700090

反应信息

  • 作为反应物:
    描述:
    1,1,1-三氟-3-甲基己烷-2,4-二酮 、 copper(II) acetate monohydrate 以 乙醇 为溶剂, 生成
    参考文献:
    名称:
    Some New β-Diketones Containing the Trifluoromethyl Group1a
    摘要:
    DOI:
    10.1021/ja01163a038
  • 作为产物:
    描述:
    3-pyrrolidino-2-pentene盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 17.5h, 生成 1,1,1-三氟-3-甲基己烷-2,4-二酮
    参考文献:
    名称:
    4-Dimethylamino-1-trifluoracetyl-pyridinium-trifluoracetat: Ein effizientes Reagens zur Synthese von Trifluormethyl-1,3-dicarbonyl-Verbindungen
    摘要:
    4-Dimethylamino-1-trifluoroacetylpyridinium Trifluoroacetat:烯胺 2 和 O-三甲基硅酮乙醛 4 在与标题试剂反应时发生三氟乙酰化反应,分别生成三氟乙酰基烯胺 3 和三氟甲基硅醇醚 5。化合物 3 和 5 经水解可得到三氟甲基 1,3-二酮 6 和三氟甲基 δ-酮酯 7。
    DOI:
    10.1055/s-1997-1501
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文献信息

  • Top seeding melt texture growth of NdBaCuO pellets in air
    作者:E. Guilmeau、F. Giovannelli、I. Monot-Laffez、S. Marinel、J. Provost、G. Desgardin
    DOI:10.1051/epjap:2001128
    日期:2001.3
    Most of NdBaCuO synthesis were realized under oxygen controlled melt growth (OCMG) which allows to avoid the solid solution formation. However, for industrial applications air synthesis is preferable due to its simplicity and its cost. In this work, different seeds and thermal cycles have been investigated in order to optimize the nucleation conditions for the obtention of a single domain. Several criteria have been defined for the choice of the seed. The solid solution Nd1+xBa2−xCu3Oy formed in these air synthesised samples appears in the range of x = 0.10 to 0.15, corresponding to between 60 K and 80 K. The nominal composition and the synthesis conditions (substrate, thermal treatments.) have to be accurately defined in order to avoid neodymium-rich solid solution formation.
    大部分NdBaCuO的合成是在氧控制熔融生长(OCMG)条件下实现的,这样可以避免固溶体的形成。然而,由于其简单性和成本优势,在工业应用中空气合成更受欢迎。在这项工作中,我们研究了不同的籽晶和热循环过程,以优化成核条件,从而获得单畴结构。我们为选择籽晶制定了几个标准。在这些空气合成样品中形成的固溶体Nd\(_1+x\)Ba\(_2-x\)Cu\(_3\)O\(_y\),其\(x\)值在0.10到0.15之间,对应的转变温度为60K到80K。为避免富钕固溶体的形成,必须准确地定义标称组成和合成条件(衬底、热处理等)。
  • Synthesis of<i>meta</i>-substituted anilines<i>via</i>a three-component reaction of acetone, amines, and 1,3-diketones
    作者:Andrew R. Galeev、Maksim V. Dmitriev、Ivan G. Mokrushin、Irina V. Mashevskaya、Andrey N. Maslivets、Michael Rubin
    DOI:10.1039/c9ob02120e
    日期:——
    facile method for the synthesis of meta-substituted arylamines from acyclic precursors was developed. This method is based on three-component cyclo-condensation/aromatization of in situ generated imines of acetone with 1,3-diketones either under conventional heating or under microwave irradiation. The utility of this methodology is illustrated by the possibility of a gram scale synthesis of various anilines
    开发了一种从无环前体合成间位取代芳基胺的简便方法。该方法基于在常规加热或微波辐射下,将原位生成的丙酮亚胺与1,3-二酮进行三组分环缩合/芳构化。这种方法的实用性可以通过从容易获得的试剂中克合成各种苯胺的可能性来说明。
  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: Cu: MVol.B4, 68, page 1589 - 1590
    作者:
    DOI:——
    日期:——
  • IRIDIUM COMPLEX PRODUCTION METHOD
    申请人:TANAKA KIKINZOKU KOGYO K.K.
    公开号:US20170253623A1
    公开(公告)日:2017-09-07
    A method for manufacturing tris(β-diketonato)iridium by reacting β-diketone with an iridium compound, in which an activation treatment including (a) an alkali treatment and (b) an acid treatment described below is applied to the iridium compound to activate the iridium compound, and to subsequently react the β-diketone, (a) an alkali treatment: a treatment of adding alkali to a solution of the iridium compound to raise pH of the solution to a more alkaline side than that before the alkali addition and to not less than 10, and (b) an acid treatment: a treatment of adding acid to the solution subjected to the alkali treatment to lower pH of the solution to a more acidic side than that before the acid addition and to make the pH difference between solutions before and after the acid addition be not less than 0.1 and not more than 10. The present invention allows manufacture of tris(β-diketonato)iridium utilizing a wide variety of β-diketones.
  • Some New β-Diketones Containing the Trifluoromethyl Group<sup>1a</sup>
    作者:J. C. Reid、M. Calvin
    DOI:10.1021/ja01163a038
    日期:1950.7
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