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4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid | 166824-91-5

中文名称
——
中文别名
——
英文名称
4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid
英文别名
1,2,3,4-tetrakis(4'-carboxyphenyl)cyclobutane;1r.2c.3t.4t-tetrakis-(4-carboxy-phenyl)-cyclobutane;TCCB;1r.2c.3t.4t-Tetrakis-(4-carboxy-phenyl)-cyclobutan
4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid化学式
CAS
166824-91-5
化学式
C32H24O8
mdl
——
分子量
536.538
InChiKey
JXAWTPKXSGKJJS-PCYFZWJMSA-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:
    761.0±60.0 °C(Predicted)
  • 密度:
    1.420±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.93
  • 重原子数:
    40.0
  • 可旋转键数:
    8.0
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    149.2
  • 氢给体数:
    4.0
  • 氢受体数:
    4.0

上下游信息

  • 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:
    4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid氯化亚砜N,N-二甲基甲酰胺 作用下, 以 二氯甲烷 为溶剂, 反应 48.0h, 生成 tetrakis(4-cyanophenyl) 4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoate
    参考文献:
    名称:
    双色4,4',4'',4'''-(环丁烷-1,2,3,4-四基)-四苯甲酸酯电致变色材料,具有较大的光学对比度和着色效率†
    摘要:
    已经设计,合成和表征了9种4,4',4'',4'''-(环丁烷-1,2,3,4-四基)四苯甲酸酯衍生物电致变色材料。七个化合物显示出双色电致变色现象。所需的电位和有色状态受取代的影响很大。当取代基为烷基时,在-2.3V和-2.6V的施加电压下分别获得紫色和蓝色的有色状态。当取代基是具有给电子基团的苯基时,在-2.1和-2.3V的施加电压下分别获得紫色的蓝色和亮蓝色的着色状态。当取代基为具有吸电子基团的苯基时,获得单色状态和差的电致变色性能。而且,基于大多数这些化合物的电致变色器件显示出大的光学对比度,快速的响应时间,
    DOI:
    10.1039/c9nj03352a
  • 作为产物:
    参考文献:
    名称:
    Hybrid Oligonucleotides Containing Stilbene Units. Excimer Fluorescence and Photodimerization
    摘要:
    Complementary pairs of oligonucleotides in which the stilbene chromophore is incorporated either in the middle or at the end of a 10 base pair sequence have been prepared and their spectroscopic and photochemical properties investigated. The individual oligonucleotides display fluorescence spectra and photoisomerization similar to that of a model 4,4'-stilbenedicarboxamide. Variations in fluorescence quantum yield and decay times are attributed to interactions with neighboring bases. One-to-one mixtures of complementary oligonucleotides form stable duplexes with melting temperatures of 40 and 46 degrees C, respectively, for the mid-strand and terminally labeled duplexes. Duplex formation results in hyperchromism of both the nucleotide and stilbene absorption bands and the appearance of broad, long-wavelength fluorescence attributed to an excited stilbene dimer. These duplexes provide a unique opportunity for the investigation of the here-to-for elusive stilbene excimer. The long wavelength absorption bands of both duplexes are efficiently bleached upon irradiation. Bleaching is a consequence-of stereospecific stilbene [2+2] photodimerization and results In the formation of cross-linked duplexes of high thermal stability. Excimer and monomer fluorescence are found to provide a highly sensitive probe of duplex formation and dissociation.
    DOI:
    10.1021/ja00139a011
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文献信息

  • A new ligand for metal–organic framework and co-crystal synthesis: mechanochemical route to rctt-1,2,3,4-tetrakis-(4′-carboxyphenyl)-cyclobutane
    作者:Goutam Kumar Kole、Lip Lin Koh、So Young Lee、Shim Sung Lee、Jagadese J. Vittal
    DOI:10.1039/c0cc00012d
    日期:——
    A novel method to access rctt-1,2,3,4-tetrakis-(4′-carboxyphenyl)-cyclobutane in quantitative yield from an environmentally benign route is presented. The cyclobutane derivative is demonstrated as a potential candidate to serve as an organic building block for making co-crystal and MOF.
    本研究介绍了一种通过无害环境的途径获得 rctt-1,2,3,4-四(4â²-羧基基)-环丁烷的新方法。这种环丁烷生物被证明是一种潜在的候选物质,可用作制造共晶体和 MOF 的有机构件。
  • Fulton, British Journal of Pharmacology and Chemotherapy, 1948, vol. 3, p. 75,76
    作者:Fulton
    DOI:——
    日期:——
  • 257. The photochemical instability of cis- and trans-4 : 4′-diamidinostilbene
    作者:Alan J. Henry
    DOI:10.1039/jr9460001156
    日期:——
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同类化合物

二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2S,3R,4S)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基](1S,2R,3S,4R)-3,4-二(苯基)环丁烷-1,2-二羧酸酯 r-1,t-2-二甲基-t-3,c-3,4-二苯基环丁烷 r-1,t-2,c-3-三苯基-c-4-氰基环丁烷 3,4-双(4-羟基苯基)环丁烷-1,2-二羧酸 3,4-二苯基环丁烷-1,2-二羧酸 1-甲氧基-4-(2,2,3,3-四甲基环丙基)苯 1-[2,3-二甲基-4-(2,4,5-三甲氧基苯基)环丁基]-2,4,5-三甲氧基苯 (2,3,4-三苯基环丁基)苯 (1R,2S,3S,4R)-3,4-二(苯基)环丁烷-1,2-二甲酸二[(1R,2R,5S)-2-甲氧羰基-8-甲基-8-氮杂双环[3.2.1]辛烷-3-基]酯 4,9-bis(2-methoxyphenyl)-3a,4,9,9a-tetrahydro-1H-4,9-epoxybenzo[f]isoindole-1,3(2H)-dione (2S,3R)-1-(Hydroxy-phenyl-methyl)-2,3-diphenyl-4-[1-phenyl-meth-(E)-ylidene]-cyclobutanol 2,3,5,6-Tetraphenyl-1,4-cyclohexandion (1S,2S,3S,4S)-3,4-Bis-[2-(di-p-tolyl-phosphinoyl)-phenyl]-cyclobutane-1,2-dicarboxylic acid diethyl ester endo-1,2-dicarbomethoxy-5,5-dimethyl-exo-3,4-diphenylbicyclo<2.1.0>pentane 2-Methylen-3,4-dihydroxy-trans-5,6-diphenylbicyclo<3.1.0>hexan 1,1,4,4-Tetramethyl-2,3b,5,6b-tetraphenyl-1,3a,3b,4,6a,6b-hexahydro-1,4-digerma-cyclobutadicyclopentene 6-Ethyl-2,6-diphenyl-bicyclo[3.1.0]hexane (1S,2S,4R,5R)-1,2,4,5-Tetraphenyl-tricyclo[3.1.0.02,4]hexane (4R,5S)-4-(3,4-dimethoxyphenyl)-5-nitro-5-(4-nitrobenzyl)tetrahydro-2H-pyran-2-one (1R,2R,3S,4S)-ethyl 1-acetyl-4-hydroxy-3-nitro-2,4-diphenylcyclopentanecarboxylate 3,4-bis-(4-hydroxy-3-methoxy-phenyl)-cyclobutane-1,2-dicarboxylic acid 1r,2c-diacetyl-3t,4t-diphenyl-cyclobutane 3,7-Diphenyl-tetracyclo<3.3.0.02,8.03,7>octan 3,3-Dimethyl-1-phenyl-tricyclo[4.1.0.02,7]heptane (3S,4R)-ethyl 1,2,3,4-tetrahydro-1-methyl-2-oxo-4-p-tolylpyridine-3-carboxylate (2R,3R)-2,3-diphenylcyclopropane-1,1-dimethanol methyl 1-formyloxy-9,9-bis(4-methoxyphenyl)pentacyclo<4.3.0.02,5.03,8.04,7>nonane-4-carboxylate (3-Cyanomethyl-2,4-diphenyl-cyclobutyl)-acetonitrile γ-Truxinsaeure (1R,6S)-1,7-Diphenyl-bicyclo[4.1.0]heptane 4,4',4'',4'''-(cyclobutane-1,2,3,4-tetrayl)tetrabenzoic acid 2,5,6-trimethyl-3,4-diphenyl-cyclohex-3-enecarboxylic acid 5,6,14,15,20,21-Hexaphenylheptacyclo<8.8.4.13,17.18,12.04,7.013,16.019,22>tetracosa-1,3(23),8,10,12(24),17-hexaen (3S,4R)-3,4-diphenyltetracyclo[11.5.0.02,5.06,12]octadeca-1,5,7,10,12,14,17-heptaene (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Ethyl 4-(7-phenyl-7-bicyclo[2.2.1]heptanyl)benzoate 5-Methyl-5,6-diphenylcyclohexa-1,3-diene 4,4',4'',4'''-cyclobutane-1,2,3,4-tetrayl-tetrakis-benzamidine (1R,2R,3S,4S)-3,4-Diphenyl-cyclobutane-1,2-dicarboxylic acid bis-dimethylamide 3,4,12,13-Tetraphenylpentacyclo<13.3.1.16,10.02,5.011,14>eicosa-1(19),6,8,10(20),15,17-hexaen 1'-[(tert-butoxy)carbonyl]-4,10-dimethyl-14,33-dinitrospiro(2,12-dioxa-18,22,25,29-tetraazahexacyclo-[29.2.2.23,6.28,11.213,16.222,25]tritetraconta-3,5,8,10,13,15,31,33,34,38,40,42-dodecaene-7,4'-piperidine)-17,30-dione 4,4'-Dibrom-β-truxinsaeure-dimethylester 1ξ-bromo-2r,3c-bis-bromomethyl-1ξ,4t-diphenyl-cyclobutane (Z)-1,2-bis(trans-2,trans-3-diphenylcyclopropyl)ethene Methyl-[3,4,4-triphenyl-thietan-(2Z)-ylidene]-amine