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4-甲基苯并-15-冠醚-5 | 32702-27-5

中文名称
4-甲基苯并-15-冠醚-5
中文别名
——
英文名称
4-methylbenzo-15-crown-5
英文别名
4'-Methylbenzo-15-krone-5;4'-Methylbenzo-15-crown-5;17-methyl-2,5,8,11,14-pentaoxabicyclo[13.4.0]nonadeca-1(15),16,18-triene
4-甲基苯并-15-冠醚-5化学式
CAS
32702-27-5
化学式
C15H22O5
mdl
——
分子量
282.337
InChiKey
HCQGDZNYDMLVRI-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
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    46.2
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:ef40c0c7032de2c43e3f9c73da6effb1
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反应信息

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文献信息

  • FLUORESCENT AROMATIC SENSORS AND THEIR METHODS OF USE
    申请人:Meador Michael A.
    公开号:US20080242870A1
    公开(公告)日:2008-10-02
    Aromatic molecules that can be used as sensors are described. The aromatic sensors include a polycyclic aromatic hydrocarbon core with a five-membered imide rings fused to the core and at least two pendant aryl groups. The aromatic sensor molecules can detect target analytes or molecular strain as a result of changes in their fluorescence, in many cases with on-off behavior. Aromatic molecules that fluoresce at various frequencies can be prepared by altering the structure of the aromatic core or the substituents attached to it. The aromatic molecules can be used as sensors for various applications such as, for example, the detection of dangerous chemicals, biomedical diagnosis, and the detection of damage or strain in composite materials. Methods of preparing aromatic sensor molecules are also described.
    描述了可以用作传感器的芳香分子。这些芳香传感器包括一个多环芳烃核心,该核心上融合了一个五元咪唑环,并且至少有两个侧链芳基基团。这些芳香传感器分子可以通过它们的荧光变化来检测目标分析物或分子应变,许多情况下具有开关行为。可以通过改变芳香核心的结构或连接到其上的取代基来制备在不同频率下发出荧光的芳香分子。这些芳香分子可以用作各种应用的传感器,例如检测危险化学品、生物医学诊断以及复合材料中的损伤或应变的检测。还描述了制备芳香传感器分子的方法。
  • An Efficient Synthetic Method for Phenylalanine Containing Crown Ether Ring
    作者:Xia Tian、Fang Li、Jianrong Han、Xiaoli Zhen、Shouxin Liu
    DOI:10.2174/157017812801264665
    日期:2012.5.1
    An efficient, convenient synthesis method has been introduced for the preparation of phenylalanine containing crown ether ring by nucleophilic substitution, nitrosation and reduction reaction using benzo-crown ether and dimethyl malonate as material. The structures of the product are characterized by 1HNMR, MS and element analysis.
    本研究介绍了一种高效、简便的合成方法,即以苯并冠醚丙二酸二甲酯为原料,通过亲核取代、亚硝基化和还原反应制备含冠醚环的苯丙酸。产品结构通过 1HNMR、MS 和元素分析进行表征。
  • Benzo-15-crown-5–Aluminium Chloride Complexes of Unusual Stability
    作者:Fumio Wada、Tsutomu Matsuda
    DOI:10.1246/bcsj.53.421
    日期:1980.2
    Among twelve crown ethers of 12, 15, 18, and 21 rings only benzo-15-crown-5 and those with an electron-releasing substituent formed the complexes with aluminium chloride which were stable in methanol.
    在 12、15、18 和 21 个环的 12 种冠醚中,只有苯并-15-冠醚-5 和具有电子释放取代基的冠醚化铝形成了在甲醇中稳定的络合物。
  • Complexes of platinum metals with crown ethers containing tertiary phosphine-substituted benzo groups
    作者:Eileen M. Hyde、Bernard L. Shaw、Ian Shepherd
    DOI:10.1039/dt9780001696
    日期:——
    to give [[graphic omitted]Ph2-2)(OMe)2-4,5}2Cl2](8; R = Ph, M = Pd). The complex [PdCl2(NCPh)2] with the bulky crown phosphine Q′ gives a mixture of trans-[PdCl2Q′2] and the corresponding cyclometallated complex; the complex (8; R = But, M = Pd) has also been prepared. A similar but more extensive series of platinum complexes has been made including mononuclear species formed by splitting the chloride-bridged
    描述了在芳烃环中取代的一些苯并-冠醚,例如一些15-X-取代的苯并-[15-冠-5]醚[1; 1; 2,3,3,4,5,6,5,6,5,6]。X = I,CHO,CH 2 OH,CH 2 CI,CH 2 Ph 2(Q)或CH 2 PBu t 2(Q')]:18-碘苯并-[18-crown-6](2; X =还描述了I)和15--16-甲基苯并-[15-crown-51](3; X = I)。但是,我们未能进行化或制备苯并冠醚的格利雅(Grignard)衍生物。模型膦PR 2 [C 6 H 3(OMe)2 -3.4] [4; R = Ph(L)或Bu t(L')]也已经合成。Li [AlH 4]还原(1; X = CHO)除了(1; X = CH 2 OH)以外,还给出二冠醚二苄基醚衍生物(5; X = H)。15-甲酰基-16-甲基苯并-[15-crown-5](3; X = CHO)
  • ANTIALLERGIC AGENTS
    申请人:Muto Susumu
    公开号:US20080090779A1
    公开(公告)日:2008-04-17
    A medicament for the preventive and/or therapeutic treatment of allergic diseases and/or endometriosis and/or hysteromyoma which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种预防和/或治疗过敏性疾病和/或子宫内膜异位症和/或子宫肌瘤的药物,其包括以下通式(I)所表示的化合物或其药学上可接受的盐、合物和溶剂化物作为活性成分,其中X表示连接基,其主链中原子数为2至5(该连接基可以被取代),A表示氢原子或乙酰基,E表示芳基或取代的杂芳基,环Z表示苯环,除了由公式-O-A表示的基团,该苯环还可以具有一个或多个取代基团,其中A的含义与上述定义相同,而由公式-X-E表示的基团中,每个X和E的含义也与上述定义相同,或者是一个杂环,除了由公式-O-A表示的基团,该杂环还可以具有一个或多个取代基团,其中A的含义与上述定义相同,而由公式-X-E表示的基团中,每个X和E的含义也与上述定义相同。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
cnmr
ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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