摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,3,5-tris(4-hydroxy-3-methoxycarbonylphenyl)benzene | 117025-64-6

中文名称
——
中文别名
——
英文名称
1,3,5-tris(4-hydroxy-3-methoxycarbonylphenyl)benzene
英文别名
6,6',6''-trihydroxy-3,3',3''-benzene-1,3,5-triyl-tri-benzoic acid trimethyl ester;6,6',6''-Trihydroxy-3,3',3''-benzen-1,3,5-triyl-tri-benzoesaeure-trimethylester;Dimethyl 4,4''-dihydroxy-5'-(4-hydroxy-3-(methoxycarbonyl)phenyl)-[1,1':3',1''-terphenyl]-3,3''-dicarboxylate;methyl 5-[3,5-bis(4-hydroxy-3-methoxycarbonylphenyl)phenyl]-2-hydroxybenzoate
1,3,5-tris(4-hydroxy-3-methoxycarbonylphenyl)benzene化学式
CAS
117025-64-6
化学式
C30H24O9
mdl
——
分子量
528.515
InChiKey
JHPIOMVGLHTNMH-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):
    6.9
  • 重原子数:
    39
  • 可旋转键数:
    9
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    140
  • 氢给体数:
    3
  • 氢受体数:
    9

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1,3,5-tris(4-hydroxy-3-methoxycarbonylphenyl)benzene 在 lithium aluminium tetrahydride 、 sodium azide 、 三溴化磷caesium carbonate红铝 作用下, 以 四氢呋喃N,N-二甲基甲酰胺丙酮甲苯 为溶剂, 反应 30.25h, 生成 [5-[3,5-bis[3-(aminomethyl)-4-butoxyphenyl]phenyl]-2-butoxyphenyl]methanamine
    参考文献:
    名称:
    Squaramido-Based Receptors:  Design, Synthesis, and Application to the Recognition of Tetraalkylammonium Compounds
    摘要:
    A new series of tripodal receptors based on squaramido rings as unprecedented binding units has been devised. Among the different structural possibilities that this functionality offers, the ability of establishing multiple O to C-H interactions has been explored. On this basis, new receptors capable of recognizing choline, acetylcholine, and related ammonium salts have been synthesized. Association constants in the range 10(3)-10(4) M(-1) have been measured by a H-1-NMR titration method The formation of intracavity complexes is supported by the observation of characteristic changes in the NMR spectra of the complexes, of intermolecular cross peaks in 2D. ROESY experiments, and by detection of signals corresponding to the molecular weight of the complexes by positive FAB mass spectrometry.
    DOI:
    10.1021/jo9614147
  • 作为产物:
    描述:
    5-乙酰水杨酸甲酯四氯化硅 作用下, 以 乙醇 为溶剂, 反应 15.0h, 以87%的产率得到1,3,5-tris(4-hydroxy-3-methoxycarbonylphenyl)benzene
    参考文献:
    名称:
    Dual Binding Mode of Methylmethanetriacetic Acid to Tripodal Amidopyridine Receptors
    摘要:
    A series of tripodal amidopyridine receptors capable of selective recognition of methylmethanetriacetic acid (MMTA) in organic solvents is described. Intramolecular hydrogen-bonding groups, built into some of the receptors, were designed as preorganization devices. Binding was studied by NMR titration, variable temperature NMR experiments, 2D-NMR, isothermal titration calorimetry, and single-crystal X-ray crystallography. The results reveal that a balancing act between inter- and intramolecular hydrogen-bonding interactions in the complexes governs both the dynamics and the geometry of binding. Receptor 1b (without intramolecular hydrogen-bonding groups) features a simple symmetric MMTA binding geometry with optimal enthalpic interactions. In sharp contrast, receptor 1a (with intramolecular hydrogen-bonding groups) reveals a temperature-dependent dual binding mode where MMTA can bind in two completely different geometries. The two solution binding geometries of 1a.AMTA were unraveled by NMR experiments and correlated to the X-ray structures.
    DOI:
    10.1021/jo025787l
点击查看最新优质反应信息

文献信息

  • Influence of remote intramolecular hydrogen bonds on the thermodynamics of molecular recognition of cis-1,3,5-cyclohexanetricar☐ylic acid
    作者:Pablo Ballester、Antoni Costa、Pere M. Deyà、Manuel Vega、Jeroni Morey、Ghislain Deslongchamps
    DOI:10.1016/s0040-4039(98)80050-6
    日期:1999.1
    thermodynamics of molecular recognition of cis-1,3,5-cyclohexanetricar☐ylic acid by tripodal hosts. Remote intramolecular hydrogen bonds, used to restrict conformationally one of the hosts, exhibit a strong influence on the thermodynamic functions for the binding process ΔH and ΔS, with little effect on ΔG. This suggests that the conformational lock imposed by the intramolecular hydrogen bonds organizes the
    利用可变温度结合研究和等温滴定微量热法,探讨了三脚架宿主对顺式-1,3,5-环己烷三丁酸酯酸的分子识别的热力学。远程分子内氢键(用于构象地限制主体之一)对结合过程ΔH和ΔS的热力学功能表现出很大的影响,而对ΔG的影响很小。这表明由分子内氢键施加的构象锁将受体组织为对于三酸的结合而言不是最佳的构象。
  • Squaramide-based receptors: Synthesis and application to the recognition of polyalkyl ammonium salts
    作者:Salvador Tomàs、M.Carmen Rotger、JoséF. González、Pere M. Deyà、Pablo Ballester、Antoni Costa
    DOI:10.1016/0040-4039(95)00297-p
    日期:1995.4
    The design and synthesis of a novel series of receptors based on mixed squaric acid diamides subunits are reported. The use of the new tripodands as receptors for several tetraalkyl ammonium salts in chloroform was studied and the resulting complexes were characterized by NMR and FAB mass analysis.
  • Molecular recognition of cis-1,3,5-cyclohexane tricarboxylic acid
    作者:Pablo Ballester、Antoni Costa、Pere M. Deyà、José F. González、M.Carmen Rotger、Ghislain Deslongchamps
    DOI:10.1016/s0040-4039(00)73106-6
    日期:1994.5
    The design and synthesis of a new receptor designed to bind tricarboxylic acids in organic solvents is described. The properties of the complex formed between the new receptor and cis-1,3,5-cyclohexanetricarboxylic acid are studied.
  • A ‘naked-eye’ chemosensor system for phytate
    作者:Jeroni Morey、Maria Orell、Miquel Àngel Barceló、Pere M. Deyà、Antoni Costa、Pablo Ballester
    DOI:10.1016/j.tetlet.2003.11.125
    日期:2004.2
    We report the synthesis of two new anion receptors of a covalently linked 1, 3,5-triarylbenzoamido-crown ether. Our results show that combined with a picrate salt they act by means of an intermolecular charge transfer process (EDA complex), as naked-eye sensors for basic anions, especially for sodium phytate in DMSO/HO2 (1:1). (C) 2003 Elsevier Ltd. All rights reserved.
  • Ballester Pablo, Costa Antoni, Deya Pere M., Gonzalez Jose F., Rotger M. +, Tetrahedron Lett, 35 (1994) N 22, S 3813-3816
    作者:Ballester Pablo, Costa Antoni, Deya Pere M., Gonzalez Jose F., Rotger M. +
    DOI:——
    日期:——
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫 龙胆紫 齐达帕胺 齐诺康唑 齐洛呋胺 齐墩果-12-烯[2,3-c][1,2,5]恶二唑-28-酸苯甲酯 齐培丙醇 齐咪苯 齐仑太尔 黑染料 黄酮,5-氨基-6-羟基-(5CI) 黄酮,6-氨基-3-羟基-(6CI) 黄蜡,合成物 黄草灵钾盐