150443-85-9 Usage
Description
Biphenyl-3,3',5,5'-tetracarbaldehyde is a chemical compound characterized by its molecular formula C20H14O4. It is a highly reactive organic compound distinguished by its four aldehyde groups. This versatile intermediate is recognized for its unique structure and reactivity, which positions it as a significant building block in organic synthesis for the creation of complex organic molecules.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 150443-85-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,4,4 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 150443-85:
(8*1)+(7*5)+(6*0)+(5*4)+(4*4)+(3*3)+(2*8)+(1*5)=109
109 % 10 = 9
So 150443-85-9 is a valid CAS Registry Number.
150443-85-9Relevant articles and documents
Inducing Social Self-Sorting in Organic Cages To Tune The Shape of The Internal Cavity
Abet, Valentina,Szczypiński, Filip T.,Little, Marc A.,Santolini, Valentina,Jones, Christopher D.,Evans, Robert,Wilson, Craig,Wu, Xiaofeng,Thorne, Michael F.,Bennison, Michael J.,Cui, Peng,Cooper, Andrew I.,Jelfs, Kim E.,Slater, Anna G.
supporting information, p. 16755 - 16763 (2020/07/21)
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.
3,3′,5,5′ tetra(phosphaalkene) biphenyl: Synthesis of a novel bicyclometalating bridging ligand, and structure of its dipalladium complex
Jouaiti, Abdelaziz,Geoffroy, Michel,Bernardinelli, Gerald
, p. 3413 - 3416 (2007/10/02)
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
