4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸
合成应用 用途与合成方法 MSDS 4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸价格(试剂级) 上下游产品信息
| 中文名称 | 4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸 |
|---|---|
| 中文同义词 | 4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸;4,4',4'',4''',4'''',4'''''-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-六基)六苯甲酸;2,3,6,7,14,15-六(4-羧基苯基)三蝶烯;六(4-羧基苯基)三蝶烯;4,4',4'',4''',4'''',4'''''-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸;hexayl)hexabenzoicacid |
| 英文名称 | 4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenoanthracene-2,3,6,7,14,15-hexayl)hexabenzoic acid |
| 英文同义词 | 4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenoanthracene-2,3,6,7,14,15-hexayl)hexabenzoic acid;4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenoanthracene-2,3,6,7,14,15-hexayl)...;2,3,6,7,14,15-hexakis(4-carboxyphenyl)triptycene;Benzoic acid, 4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10[1',2']-benzenoanthracene-2,3,6,7,14,15-hexayl)hexakis-;4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-dihydro-9,101′,2′-benzenoanthracene-2,3,6,7,14,15-hexayl)hexakis- (ACI) Benzoic acid;4,4',4'',4''',4'''',4'''''-(9,10-dihydro-9,10-[1,2]benzenebenzoanthracene-2,3,6,7,14,15-hexayl)hexabenzenemacetic acid |
| CAS号 | 1835723-11-9 |
| 分子式 | C62H38O12 |
| 分子量 | 974.97 |
| EINECS号 | |
| 相关类别 | |
| Mol文件 | 1835723-11-9.mol |
| 结构式 | ![4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸 结构式](CAS/20211123/GIF/1835723-11-9.gif) |
4,4′,4′′,4′′′,4′′′′,4′′′′′-(9,10-二氢-9,10-[1,2]苯并蒽-2,3,6,7,14,15-己基)六苯甲酸 性质
| 密度 | 1.435±0.06 g/cm3(Predicted) |
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| 储存条件 | Store at room temperature |
| 酸度系数(pKa) | 3.33±0.10(Predicted) |
| 外观 | 白色至灰白色固体 |
| InChIKey | PZUNVLJATCTESM-UHFFFAOYSA-N |
可作为配体用于合成MOF材料:NU-1500-Cr/Cr-acs-MOF
[2] Interpenetration Isomerism in Triptycene‐Based Hydrogen‐Bonded Organic Frameworks. https://doi.org/10.1002/anie.201811263
[3] Reticular Access to Highly Porous acs-MOFs with Rigid Trigonal Prismatic Linkers for Water Sorption. https://doi.org/10.1021/jacs.8b13710
参考文献
[1] Preparation of Tri‐ and Hexasubstituted Triptycene Synthons by Transition Metal Catalyzed Cross‐Coupling Reactions for Post‐Modifications. https://doi.org/10.1002/ejoc.201501272
[2] Interpenetration Isomerism in Triptycene‐Based Hydrogen‐Bonded Organic Frameworks. https://doi.org/10.1002/anie.201811263
[3] Reticular Access to Highly Porous acs-MOFs with Rigid Trigonal Prismatic Linkers for Water Sorption. https://doi.org/10.1021/jacs.8b13710