Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Chemical Reagents >  Organic reagents >  Cyclodextrin >  1,2,4,5-Tetrakis(4-carboxyphenyl)benzene

1,2,4,5-Tetrakis(4-carboxyphenyl)benzene

Basic information Safety Supplier Related

1,2,4,5-Tetrakis(4-carboxyphenyl)benzene Basic information

Product Name:
1,2,4,5-Tetrakis(4-carboxyphenyl)benzene
Synonyms:
  • H4TCPB
  • 1,2,4,5-Tetrakis(4-carboxyphenyl)benzene contains up to 6 wt. % water, >=98%
  • 1,2,4,5-Tetrakis(4-carboxyphenyl)benzene
  • 4',5'-Bis(4-carboxyphenyl)-[1,1':2',1''-terphenyl]-4,4''-dicarboxylic acid
  • 4,4',4'',4'''-benzene-1,2,4,5-tetrayl-tetrabenzoic acid
  • [1,1':2',1''-Terphenyl]-4,4''-dicarboxylic acid, 4',5'-bis(4-carboxyphenyl)-
  • 1,2,4,5-Tetrakis(4-carboxyphenyl)benzene (This product is unavailable in the U.S.)
  • DK7240
CAS:
1078153-58-8
MF:
C34H22O8
MW:
558.53
Mol File:
1078153-58-8.mol
More
Less

1,2,4,5-Tetrakis(4-carboxyphenyl)benzene Chemical Properties

Boiling point:
792.8±60.0 °C(Predicted)
Density 
1.393±0.06 g/cm3(Predicted)
Flash point:
85 °C
pka
3.24±0.10(Predicted)
More
Less

1,2,4,5-Tetrakis(4-carboxyphenyl)benzene Usage And Synthesis

Uses

Selected Applications of MOFs in Sustainable Energy Technologies

General Description

This product has been enhanced for energy efficiency.

Synthesis


a) 100 ml of p-tolylmagnesium bromide (1M in THF, 100 mmol) was added under nitrogen to a flask containing 5g of (9.07 mmol). The mixture was stirred at nitrogen to a flask containing 5g of (9.07 mmol). The mixture was stirred at room temperature for 15 hours (gray suspension). The reaction was poured on ice then 50 ml of 6M HCl was added. The mixture was extracted with THF (3X 200ml). The organics were combined and the solvent was removed via rotary evaporation. The solid was then washed with hexanes and cold acetone. Isolated yield: 2.75g, 70% based on hexabromobenzene. yield: 2.75g, 70% 1H NMR (CDCl3): δ 2.32 (s, 12H), 7.04 (d, 8H), 7.12 (d, 8H), 7.45 (s, 2H). 13C NMR (CDCl3): δ 128.9, 130.0, 133.3, 136.4, 138.4, 139.5 ppm.(b) An amount of 2g from (a) was placed in a 100 ml teflon lined vessel. An amount of 24 ml of water and 6 ml of HNO3 were then added. The vessel was sealed and heated at 180 °C for 24 hrs. The resulting solid was collected by filtration and washed with THF/CHCl3 (7:3). Isolated yield: 1.85g, 75%. yield: 1.85g, 75%

1,2,4,5-Tetrakis(4-carboxyphenyl)benzeneSupplier

Anqing Donghe Biotechnology Co., Ltd Gold
Tel
15056029383
Email
product@aqdonghe.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Email
sales3.gd@hwrkchemical.com
TOKYO CHEMICAL INDUSTRY CO., LTD.
Tel
03-36680489
Email
Sales-JP@TCIchemicals.com
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Email
product02@bidepharm.com
Shanghai DiBai Chemicals Co., Ltd.
Tel
021-54359730 400-008-9730
Email
info@chemxyz.com