645401-15-6

Basic information

• Product Name: 1,3,5,7-tetrakis-(4-formylphenyl)adamantane
• Synonyms: 1,3,5,7-tetrakis-(4-formylphenyl)adamantane
• CAS NO: 645401-15-6
• Molecular Weight: 552.67
• Mol File: 645401-15-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 735.0±60.0 °C(Predicted)
• Density: 1.309±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,3,5,7-tetrakis-(4-formylphenyl)adamantane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5,7-tetrakis-(4-formylphenyl)adamantane(645401-15-6)
• EPA Substance Registry System: 1,3,5,7-tetrakis-(4-formylphenyl)adamantane(645401-15-6)

Safety Data

• Hazardous Substances Data: 645401-15-6(Hazardous Substances Data)

Usage

General Description

1,3,5,7-tetrakis-(4-formylphenyl)adamantane is a chemical compound with the molecular formula C40H32O4. It is a symmetrical organic compound featuring four benzene rings attached to a central adamantane core, with each benzene ring containing a formyl group (-CHO). 1,3,5,7-tetrakis-(4-formylphenyl)adamantane has potential applications in materials science, organic synthesis, and pharmaceuticals due to its unique structure and properties. It has been studied for its potential use in the development of new materials with enhanced properties, as well as its potential as a building block for the synthesis of complex organic molecules. 1,3,5,7-tetrakis-(4-formylphenyl)adamantane is of interest to researchers for its potential applications in a wide range of fields, including chemistry, materials science, and pharmaceuticals.

Upstream product

• 4885-02-3 Dichloromethyl methyl ether 
• 16004-75-4 1,3,5,7-tetrakis(phenyl)adamantane 

Downstream Products

• 947369-36-0 C₈₆H₇₂N₁₆ 

Relevant articles and documents

Synthesis and use of a hyper-connecting cross-linking agent in the hole-transporting layer of perovskite solar cells

Solution-processed organic semiconducting materials feature prominently in modern optoelectronic devices, especially where low-cost and flexibility are specific goals, such as perovskite solar cells. Their intrinsic solubility, poor cohesion and lack of a

Micro- and mesoporous poly(Schiff-base)s constructed from different building blocks and their adsorption behaviors towards organic vapors and CO2 gas

Four porous poly(Schiff-base)s, PSN-DA, PSN-TAPB, PSN-TAPA and PSN-TAPM, are synthesized via one-pot condensation from 1,3,5,7-tetrakis(4-formylphenyl)adamantane with rod-like m-phenyldiamine, triangular 1,3,5-tris(4-aminophenyl)benzene and tris(4-aminophenyl)amine as well as tetrahedral tetrakis(4-aminophenyl)methane, respectively. It is found that the variation of the geometrical shape of the building blocks significantly alters the surface areas, pore sizes and distributions of the resultant porous polymers and thereby remarkably influences their adsorption behaviors towards organic vapors and CO2 gas. PSN-DA, PSN-TAPB and PSN-TAPA are microporous materials with pore sizes of 0.72, 0.95 and 1.04 nm, whereas PSN-TAPM is a micro- and mesoporous material with the major pores centered at 0.86 and 2.62 nm, respectively. Their BET surface areas are in the range from 419 to 1045 m2 g-1. At P/Po = 0.9 and 298 K, PSN-DA possesses high uptakes for both aromatic vapor (benzene, 86.1 wt%) and aliphatic vapor (cyclohexane, 77.9 wt%). In addition, the adsorption and desorption isotherms of CO2 gas in the four porous polymers are reversible-a characteristic which is convenient for the regeneration of CO2 adsorbents. Their adsorption capacities of CO2 are up to 15.0 wt% (273 K/1 bar) with the ideal selectivities of CO2/N2 and CO2/CH4 up to 71 and 14, respectively. showing potential applications in the removal of toxic organic vapors and capture of CO2 from air.