185252-69-1 Usage
Uses
Used in Pharmaceutical Industry:
4-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-BENZOIC ACID is used as a key intermediate in the synthesis of pharmaceuticals for its potential biological activities. It contributes to the development of new drugs by serving as a structural component that can be modified to enhance pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-BENZOIC ACID is employed as a versatile building block. Its reactivity and structural features allow for the creation of a diverse array of organic compounds, facilitating advancements in material science, agrochemicals, and other chemical-based industries.
Used in Drug Discovery:
4-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-BENZOIC ACID is utilized as a starting point in drug discovery processes. Its unique structure provides a foundation for the design and optimization of novel therapeutic agents, potentially leading to the development of new treatments for various diseases and conditions.
Used in Medicinal Chemistry Research:
In medicinal chemistry research, 4-(3,5-DIMETHYL-1H-PYRAZOL-4-YL)-BENZOIC ACID is applied as a valuable tool for studying the structure-activity relationships of biologically active molecules. Its incorporation into various chemical entities aids researchers in understanding the molecular mechanisms underlying their biological effects, thereby guiding the optimization of drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 185252-69-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,2,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 185252-69:
(8*1)+(7*8)+(6*5)+(5*2)+(4*5)+(3*2)+(2*6)+(1*9)=151
151 % 10 = 1
So 185252-69-1 is a valid CAS Registry Number.
185252-69-1Relevant academic research and scientific papers
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.
, 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
The synthesis and characterisation of coordination and hydrogen-bonded networks based on 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoic acid
Bryant, MacGuire R.,Burrows, Andrew D.,Fitchett, Christopher M.,Hawes, Chris S.,Hunter, Sally O.,Keenan, Luke L.,Kelly, David J.,Kruger, Paul E.,Mahon, Mary F.,Richardson, Christopher
, p. 9269 - 9280 (2015/05/20)
The synthesis, structural and thermal characterisation of a number of coordination complexes featuring the N,O-heteroditopic ligand 4-(3,5-dimethyl-1H-pyrazol-4-yl)benzoate, HL are reported. The reaction of H2L with cobalt(II) and nickel(II) ni
