1325728-09-3 Usage
Uses
Used in Coordination Chemistry:
1,3,5-tris(1H-pyrazol-4-yl)benzene is used as a ligand for [forming stable bonds with metal ions] due to [its ability to create strong, stable bonds with metal ions, contributing to the stability and functionality of metal-organic frameworks and coordination polymers].
Used in the Design of Metal-Organic Frameworks (MOFs):
1,3,5-tris(1H-pyrazol-4-yl)benzene is used as a building block for [constructing complex supramolecular structures] because of [its unique structure that allows for versatile interactions with metal ions, enhancing the design of MOFs with tailored properties].
Used in the Development of New Materials:
1,3,5-tris(1H-pyrazol-4-yl)benzene is used as a component in [creating new materials with potential applications in various fields] for [its contribution to the development of materials with specific properties, such as those needed for gas storage, sensing, or other specialized uses].
Used in Catalyst Design:
1,3,5-tris(1H-pyrazol-4-yl)benzene is used as a key element in [designing catalysts with enhanced performance] for [its role in forming active sites in catalysts, potentially improving their efficiency and selectivity in various chemical reactions].
Check Digit Verification of cas no
The CAS Registry Mumber 1325728-09-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,5,7,2 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1325728-09:
(9*1)+(8*3)+(7*2)+(6*5)+(5*7)+(4*2)+(3*8)+(2*0)+(1*9)=153
153 % 10 = 3
So 1325728-09-3 is a valid CAS Registry Number.
1325728-09-3Relevant articles and documents
Preparation method of pyrazole-4-aryl derivative
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Paragraph 0019, (2019/01/07)
The invention discloses a preparation method of a pyrazole-4-aryl derivative. The preparation method comprises the following step: mixing an aryl halide derivative, a pyrazole-4-boronic acid pinacol ester derivative, first alkali, a first phase transfer catalyst and a first palladium-based catalyst in a first solvent to carry out reaction so as to prepare the pyrazole-4-aryl derivative. Through the manner, the pyrazole-4-aryl derivative is prepared through the adoption of a one-pot method; the reaction condition is mild and the post-treatment is simple and convenient, so that the method is suitable for multiple aryl halide derivatives, strong in operability and suitable for industrial production; and the obtained pyrazole compound can be widely applied to the field of chemical engineering,medicines, biology and materials.
Efficient and chromatography-free methodology for the modular synthesis of oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk
Kershaw Cook, Laurence J.,Kearsey, Rachel,Lamb, Jessica V.,Pace, Edward J.,Gould, Jamie A.
supporting information, p. 895 - 898 (2016/02/05)
A novel methodology to synthesise oligo-(1H-pyrazol-4-yl)-arenes with controllable size, shape and steric bulk from 1-trityl-1H-pyrazol-4-ylboronate pinacol esters. This straightforward and efficient procedure can be applied to a variety of brominated aro
