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1,5-二甲基-2-金刚烷酮 | 33794-98-8

中文名称
1,5-二甲基-2-金刚烷酮
中文别名
——
英文名称
1,5-Dimethyl-2-adamantanone
英文别名
dimethyl-1,5 adamantanone-2;3.5-Dimethyl-2-adamantanon;1,5-dimethyl-adamantanone;1,3-dimethyl-4-adamantanone;1,5-dimethyladamantan-2-one
1,5-二甲基-2-金刚烷酮化学式
CAS
33794-98-8
化学式
C12H18O
mdl
——
分子量
178.274
InChiKey
FAQCWWQDIFCGEM-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):
    2.5
  • 重原子数:
    13
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.92
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Methods of acylating adamantane, tricyclo[5.2.1.02,6], and decalin compounds
    申请人:Daicel Chemical Industries, Ltd.
    公开号:US06429314B1
    公开(公告)日:2002-08-06
    An acylating agent of the invention includes (A) a 1,2-dicarbonyl compound or its hydroxy reductant, (B) oxygen, and (C) at least one compound selected from (c1) a metallic compound and (C2) N-hydroxyphthalimide or another imide compound. As the 1,2-dicarbonyl compound or its hydroxy reductant (A), biacetyl, 2,3-butanediolor the like canbeused. As the metallic compound (c1), cobalt acetate, or another cobalt compound, for example, can be employed. By reacting an adamantane derivative or another compound having a methine carbon atom with the acylating agent, an acyl group can be introduced to the methine carbon atom with efficiency.
    本发明的酰化剂包括(A)1,2-二羰基化合物或其羟基还原剂,(B)氧气,以及(C)至少选择自(c1)金属化合物和(C2)N-羟基邻苯二甲酰亚胺或另一种亚胺化合物的化合物。作为1,2-二羰基化合物或其羟基还原剂(A),可以使用双醋酸、2,3-丁二醇等。作为金属化合物(c1),可以采用乙酸钴或另一种钴化合物。通过将金刚烷衍生物或另一种具有亚甲基碳原子的化合物与酰化剂反应,可以高效地在亚甲基碳原子上引入酰基。
  • ACYLATING AGENTS, ACYLATION METHOD WITH THE USE OF THE SAME AND ADAMANTANE DERIVATIVES
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP0990634A1
    公开(公告)日:2000-04-05
    An acylating agent of the invention includes (A) a 1,2-dicarbonyl compound or its hydroxy reductant, (B) oxygen, and (C) at least one compound selected from (c1) a metallic compound and (C2) N-hydroxyphthalimide or another imide compound. As the 1,2-dicarbonyl compound or its hydroxy reductant (A), biacetyl, 2,3-butanediol or the like can be used. As the metallic compound (c1), cobalt acetate, or another cobalt compound, for example, can be employed. By reacting an adamantane derivative or another compound having a methine carbon atom with the acylating agent, an acyl group can be introduced to the methine carbon atom with efficiency.
    本发明的酰化剂包括(A)1,2-二羰基化合物或其羟基还原剂,(B)氧和(C)至少一种选自(c1)金属化合物和(C2)N-羟基邻苯二甲酰亚胺或另一种酰亚胺化合物的化合物。作为 1,2-二羰基化合物或其羟基还原剂 (A),可以使用生物乙酰基、2,3-丁二醇或类似物。作为金属化合物(c1),可以使用醋酸钴或其他钴化合物等。将金刚烷衍生物或其他具有甲烷碳原子的化合物与酰化剂反应,可以有效地将酰基引入甲烷碳原子。
  • 4-Oxatricyclo(4.3.1.1-3,8)undecan-5-one derivatives and process for producing the same
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP1081150A1
    公开(公告)日:2001-03-07
    A 4-oxatricyclo[4.3.1.13,8]undecan-5-one derivative is shown by the following formula (1): wherein R is a hydrogen atom or a (meth)acryloyl group, and carbon atoms constituting a ring may have a substituent in addition to the substituents indicated in the formula. This compound is a novel 4-oxatricyclo[4.3.1.13,8]undecan-5-one derivative having a hydroxyl group or a (meth)acryloyloxy group at the 1-position.
    4-oxatricyclo[4.3.1.13,8]undecan-5-one 衍生物如下式(1)所示: 其中 R 是氢原子或(甲基)丙烯酰基,而构成环的碳原子除了具有式中所示的取代基外,还可以具有一个取代基。该化合物是一种新型 4-氧杂三环[4.3.1.13,8]十一烷-5-酮衍生物,在 1 位上具有羟基或(甲基)丙烯酰氧基。
  • A remarkable effect of quaternary ammonium bromide for the N-hydroxyphthalimide-catalyzed aerobic oxidation of hydrocarbons
    作者:Katsuhisa Matsunaka、Takahiro Iwahama、Satoshi Sakaguchi、Yasutaka Ishii
    DOI:10.1016/s0040-4039(99)00139-2
    日期:1999.3
    A methodology for the aerobic oxidation of organic substrates in the absence of any metal catalyst has been established using combined catalytic system consisting of N-hydroxyphthalimide and quaternary ammonium bromide. Thus, various hydrocarbons were successfully oxidized under dioxygen atmosphere to the corresponding oxygenated compounds in good selectivities. (C) 1999 Elsevier Science Ltd. All rights reserved.
  • Drivas, Ioannis; Mison, Pierre, Bulletin de la Societe Chimique de France, 1984, vol. 2, # 5-6, p. 252 - 264
    作者:Drivas, Ioannis、Mison, Pierre
    DOI:——
    日期:——
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