1660960-30-4

Basic information

• Product Name: 1,3,5-tris(3-amino-4-carboxyphenyl)benzene
• CAS NO: 1660960-30-4
• Molecular Weight: 483.48
• Mol File: 1660960-30-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,3,5-tris(3-amino-4-carboxyphenyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tris(3-amino-4-carboxyphenyl)benzene(1660960-30-4)
• EPA Substance Registry System: 1,3,5-tris(3-amino-4-carboxyphenyl)benzene(1660960-30-4)

Safety Data

• Hazardous Substances Data: 1660960-30-4(Hazardous Substances Data)

Usage

Chemical structure

1,3,5-tris(3-amino-4-carboxyphenyl)benzene is a chemical compound with three amino and carboxy groups bound to a benzene ring at the 1, 3, and 5 positions, creating a symmetrical arrangement.

Common use

It is commonly used in organic synthesis and chemical research due to its unique structure and potential for creating complex molecules.

Building block

It can be used as a building block in the production of advanced materials, such as liquid crystals, polymers, and pharmaceuticals.

Upstream product

• 365564-05-2 1,3,5-tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene 
• 626-39-1 1,3,5-trisbromobenzene 

Relevant articles and documents

Introduction of functionality, selection of topology, and enhancement of gas adsorption in multivariate metal-organic framework-177

Metal-organic framework-177 (MOF-177) is one of the most porous materials whose structure is composed of octahedral Zn4O(-COO)6 and triangular 1,3,5-benzenetribenzoate (BTB) units to make a three-dimensional extended network based on the qom topology. This topology violates a long-standing thesis where highly symmetric building units are expected to yield highly symmetric networks. In the case of octahedron and triangle combinations, MOFs based on pyrite (pyr) and rutile (rtl) nets were expected instead of qom. In this study, we have made 24 MOF-177 structures with different functional groups on the triangular BTB linker, having one or more functionalities. We find that the position of the functional groups on the BTB unit allows the selection for a specific net (qom, pyr, and rtl), and that mixing of functionalities (-H, -NH2, and -C4H4) is an important strategy for the incorporation of a specific functionality (-NO2) into MOF-177 where otherwise incorporation of such functionality would be difficult. Such mixing of functionalities to make multivariate MOF-177 structures leads to enhancement of hydrogen uptake by 25%.