150443-85-9

Basic information

• Product Name: biphenyl-3,3',5,5'-tetracarbaldehyde
• Synonyms: biphenyl-3,3',5,5'-tetracarbaldehyde;[1,1'-Biphenyl]-3,3',5,5'-tetracarboxaldehyde;[1,1'-biphenyl]-3,3',5,5'-tetracarbaldehyde
• CAS NO: 150443-85-9
• Molecular Formula: C16H10O4
• Molecular Weight: 266.2482
• Product Categories: COF
• Mol File: 150443-85-9.mol

Chemical Properties

• Boiling Point: 527.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.322±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: biphenyl-3,3',5,5'-tetracarbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: biphenyl-3,3',5,5'-tetracarbaldehyde(150443-85-9)
• EPA Substance Registry System: biphenyl-3,3',5,5'-tetracarbaldehyde(150443-85-9)

Safety Data

• Hazardous Substances Data: 150443-85-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Biphenyl-3,3',5,5'-tetracarbaldehyde is used as a key building block in the synthesis of complex organic molecules, leveraging its high reactivity and unique structure to facilitate the formation of a wide range of compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, biphenyl-3,3',5,5'-tetracarbaldehyde is utilized as an intermediate for the development of new drugs. Its reactivity allows for the creation of diverse pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemicals:
Biphenyl-3,3',5,5'-tetracarbaldehyde also serves as an intermediate in the agrochemical industry, contributing to the synthesis of various agrochemical products designed to enhance crop protection and yield.
Used in Materials Science:
biphenyl-3,3',5,5'-tetracarbaldehyde is applied in materials science as a precursor for developing novel materials with unique properties, such as those with enhanced stability or specific optical characteristics.
Used in Organic Electronics:
Biphenyl-3,3',5,5'-tetracarbaldehyde has been studied for its potential use in organic electronics, where its properties may contribute to the development of innovative electronic devices and components.

Upstream product

• 150443-84-8 C₂₈H₃₄O₈ 
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• 120173-41-3 5-bromobenzene-1,3-dicarbaldehyde 
• 150443-83-7 C₁₄H₁₇BrO₄ 

Relevant articles and documents

Inducing Social Self-Sorting in Organic Cages To Tune The Shape of The Internal Cavity

Many interesting target guest molecules have low symmetry, yet most methods for synthesising hosts result in highly symmetrical capsules. Methods of generating lower symmetry pores are thus required to maximise the binding affinity in host–guest complexes. Herein, we use mixtures of tetraaldehyde building blocks with cyclohexanediamine to access low-symmetry imine cages. Whether a low-energy cage is isolated can be correctly predicted from the thermodynamic preference observed in computational models. The stability of the observed structures depends on the geometrical match of the aldehyde building blocks. One bent aldehyde stands out as unable to assemble into high-symmetry cages-and the same aldehyde generates low-symmetry socially self-sorted cages when combined with a linear aldehyde. We exploit this finding to synthesise a family of low-symmetry cages containing heteroatoms, illustrating that pores of varying geometries and surface chemistries may be reliably accessed through computational prediction and self-sorting.

Two-dimensional dual-pore covalent organic frameworks obtained from the combination of two: D 2h symmetrical building blocks

A strategy to construct covalent organic frameworks (COFs) bearing two different kinds of pores has been developed, by which two dual-pore COFs were fabricated through the condensation reactions of two D2h symmetrical building blocks. The COFs exhibit good adsorption capacities for CO2 and H2.

3,3′,5,5′ tetra(phosphaalkene) biphenyl: Synthesis of a novel bicyclometalating bridging ligand, and structure of its dipalladium complex

A biphenyl derivative bearing four phosphaalkene groups in positions 3,3′,5,5′ has been synthesized and is shown to be a bis-terdentate chelating agent; this novel bridging ligand forms a complex with two palladium ions and the crystal structure of this d