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1-(双环[2.2.1]庚-2-烯-2-基)乙酮 | 71720-43-9

中文名称
1-(双环[2.2.1]庚-2-烯-2-基)乙酮
中文别名
——
英文名称
(Bicyclo<2.2.1>hept-2-en-2-yl)-1-ethanon
英文别名
2-Acetylbicyclo<2.2.1>hept-2-ene;1-norborn-2-en-2-yl-ethanone;1-Norborn-2-en-2-yl-aethanon;1-bicyclo[2.2.1]hept-2-en-2-ylethan-1-one;2-Acetyl-norbornen-(2);1-Bicyclo(2.2.1)hept-2-en-2-ylethan-1-one;1-(2-bicyclo[2.2.1]hept-2-enyl)ethanone
1-(双环[2.2.1]庚-2-烯-2-基)乙酮化学式
CAS
71720-43-9
化学式
C9H12O
mdl
MFCD18806666
分子量
136.194
InChiKey
ZBKHUDFVGLNUNL-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):
    1.8
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.666
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

SDS

SDS:cd6486e2a7f22593c57542b136a3774c
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反应信息

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文献信息

  • PROCESS FOR PRODUCING HIGH PURITY EXO-ALKENYLNORBORNENE
    申请人:Bell Andrew
    公开号:US20090054714A1
    公开(公告)日:2009-02-26
    Embodiments of the present invention are directed generally to methods for producing high purity exo-alkenylnorbornenes from a mixture of conformational isomers thereof.
    本发明的实施例通常涉及从共轭异构体混合物中生产高纯度的外部烯基去氢脱环戊烷。
  • COMPOUND AND POLYMER COMPOUND CONTAINING THE COMPOUND
    申请人:JAPAN SCIENCE AND TECHNOLOGY AGENCY
    公开号:US20210002284A1
    公开(公告)日:2021-01-07
    Provided is a compound having higher fluorescence quantum yield and higher optical stability than a conventional FLAP and a polymer compound containing the compound. A: seven or eight-membered ring structure, Y 1 ,Y 2 ,Y 3 : halogen atom or the like, a1: number of Y 1 , a2: number of Y 2 , B: number of Y 3 , 0≤m and n≤3: when 1≤m≤3, Y 1 may be substituted with a structure portion defined by m, when 1≤n≤3, Y 2 may be substituted with a structure portion defined by n, and B 1 , B 2 : Formulas (2-1) to (2-3). C 1 , C 2 , C 3 : structure containing a cyclic hydrocarbon compound, D 1 , D 2 , D 3 : substructure that inhibits aggregation, E 1 , E 2 , E 3 : polymerizable substructure, Z 1 : hydrogen atom or the like, c: number of substituent groups Z 1 , Z 2 , Z 3 : hydrogen atom or the like, and may form a ring with C 2 .
    提供了一种具有比传统FLAP具有更高荧光量子产率和更高光学稳定性的化合物,以及含有该化合物的聚合物化合物。A:七元或八元环结构,Y1,Y2,Y3:卤素原子或类似物,a1:Y1的数量,a2:Y2的数量,B:Y3的数量,0≤m和n≤3:当1≤m≤3时,Y1可能被定义为m的结构部分替代,当1≤n≤3时,Y2可能被定义为n的结构部分替代,B1,B2:公式(2-1)至(2-3)。C1,C2,C3:含有环烃化合物的结构,D1,D2,D3:抑制聚集的亚结构,E1,E2,E3:可聚合的亚结构,Z1:氢原子或类似物,c:取代基Z1的数量,Z2,Z3:氢原子或类似物,可能与C2形成环。
  • Friedel-Crafts acylation of 2-trimethylsilylnorbornene. Effect of acyl group on the position of attack
    作者:Gopalpur Nagendrappa、Noor Shahina Begum
    DOI:10.1016/s0040-4020(99)00402-0
    日期:1999.6
    The acylation of 2-trimethylsilylnorbornene 1 in the presence of aluminium chloride gives minor quantities of the expected 2-norbornenyl ketones 4. The formation of 3 and 5 as major products indicates that either α-or β-attack takes place predominantly depending on the nature of the acyl group, and the β-silicon effect is not a decisive factor. The β-silyl cation intermediate 2 mainly leads to nortricyclyl
    2-三甲基甲硅烷基降冰片烯1在氯化铝存在下的酰化作用可得到少量的预期2-降冰片烯基酮4。作为主要产物的3和5的形成表明,主要取决于酰基的性质而发生α攻击或β攻击,而β硅效应不是决定性因素。β-甲硅烷基阳离子中间体2主要通过1,3-去质子化产生正三环基酮3,并且α-甲硅烷基阳离子8经历重排以产生新颖的桥头甲硅烷基化产物5。
  • Mechanochromic luminescent material, mechanochromic resin obtained by crosslinking mechanochromic luminescent material, method for producing mechanochromic luminescent material, and method for producing mechanochromic
    申请人:JAPAN SCIENCE AND TECHNOLOGY AGENCY
    公开号:US10442886B2
    公开(公告)日:2019-10-15
    Provided is a mechanochromic resin by which a stress applied to a material can be visualized in real time, and a mechanochromic luminescent material that is used in the synthesis of the mechanochromic resin. Stress can be visualized in real time by means of a mechanochromic luminescent material represented by formula (1) or formula (2) and a mechanochromic resin obtained by crosslinking the mechanochromic luminescent material. [Chemical formula 1] (In the formula, Y1 and Y2 each denote a substituent group that inhibits aggregation of the mechanochromic luminescent material represented by formula (1), and Y1 and Y2 may be same as or different from each other. Z1 and Z2 each denote a polymerizable group, and may be same as or different from each other.) [Chemical formula 2] (In the formula, Y1 and Y2 each denote a substituent group that inhibits aggregation of the mechanochromic luminescent material represented by formula (2), and Y1 and Y2 may be same as or different from each other. Z1 and Z2 each denote a polymerizable group, and may be same as or different from each other).
    提供一种机械致变色树脂,可实时可视化材料受到的应力,以及用于合成机械致变色树脂的机械致发光材料。通过公式(1)或公式(2)所表示的机械致发光材料和交联该机械致发光材料所得到的机械致变色树脂,可以实时可视化应力。【化学式1】(在公式中,Y1和Y2分别表示抑制公式(1)所表示的机械致发光材料聚集的取代基,Y1和Y2可以相同也可以不同。Z1和Z2分别表示可聚合基团,可以相同也可以不同。)【化学式2】(在公式中,Y1和Y2分别表示抑制公式(2)所表示的机械致发光材料聚集的取代基,Y1和Y2可以相同也可以不同。Z1和Z2分别表示可聚合基团,可以相同也可以不同。)
  • Catalyst system for polymerizing cyclic olefin having polar functional group, polymerizing method using the catalyst system, olefin polymer produced by the method and optical anisotropic film comprising the olefin polymer
    申请人:Yoon Cheol Sung
    公开号:US20060058477A1
    公开(公告)日:2006-03-16
    A catalyst system capable of producing a cyclic olefin polymer having a polar functional group and a high molecular weight with a high yield in which a catalyst is not deactivated due to polar functional groups of monomers, and a method of producing polymers using the same are provided. The catalyst system for polymerization of olefin according to the present invention has good thermal and chemical stability, and thus, in the method of preparing polyolefin using the catalyst system, the deactivation of a catalyst due to a polar functional group of the monomer can be prevented, and thus a high yield of the cyclic olefin polymer with a high molecular weight can be obtained when a ratio of the catalyst to the monomer is 1:5000, and the removal of a catalyst residue is not required.
    提供了一种催化剂体系,能够产生具有极性功能基和高分子量的环状烯烃聚合物,并具有高产率,其中催化剂不会因单体的极性功能基而失活,以及使用相同的聚合物生产方法。根据本发明的烯烃聚合催化剂体系具有良好的热稳定性和化学稳定性,因此,在使用该催化剂体系制备聚烯烃的方法中,可以防止由于单体的极性功能基而导致催化剂失活,因此当催化剂与单体的比例为1:5000时,可以获得高产率的具有高分子量的环状烯烃聚合物,并且不需要去除催化剂残留物。
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