851083-40-4 Usage
Molecular Structure
1H-Pyrazole-3-carboxylic acid, 4-benzoyl-1-methyl-5-phenylconsists of a pyrazole ring with a carboxylic acid group at the 3rd position, a benzoyl group at the 4th position, a methyl group at the 1st position, and a phenyl group at the 5th position.
Classification
It is a pyrazole derivative.
Molecular Weight
281.3
Appearance
Pale yellow solid.
Solubility
It is soluble in common organic solvents such as ethanol, methanol, and DMSO.
Melting Point
It has a melting point in the range of 160-162°C.
Spectroscopic Data
1H-Pyrazole-3-carboxylic acid, 4-benzoyl-1-methyl-5-phenylhas been characterized by various spectroscopic techniques such as NMR, IR, and HRMS.
Medicinal Chemistry Applications
It has potential applications in medicinal chemistry, specifically in the development of pharmaceutical drugs.
Drug Discovery and Design
Its unique structure and properties make it a promising candidate for further research and development in the field of drug discovery and design.
Check Digit Verification of cas no
The CAS Registry Mumber 851083-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,0,8 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 851083-40:
(8*8)+(7*5)+(6*1)+(5*0)+(4*8)+(3*3)+(2*4)+(1*0)=154
154 % 10 = 4
So 851083-40-4 is a valid CAS Registry Number.
851083-40-4Relevant academic research and scientific papers
Akbas, Esvet,Berber, Ismet,Sener, Ahmet,Hasanov, Beybala
, p. 23 - 26 (2005)
Some new 1H-pyrazole-3-carboxylic acid and pyridazinone derivatives were synthesized and evaluated for their antibacterial activities against Bacillus cereus ATCC 7064, Staphylococcus aureus ATCC 6538, Escherichia coli ATCC 4230 and Pseudomonas putida usi
Microwave-assisted studies on the reactions of the 4-Benzoyl-5-phenyl- 2,3-dihydro-2,3-furandione and derivatives
Akbas, Esvet,Sener, Ahmet
scheme or table, p. 103 - 105 (2010/08/05)
Varieties of heterocyclic compounds were prepared in good yield from 4-benzoyl-5-phenyl-2,3-dihydro-2,3- furandione under microwave irradiation conditions. The reaction revealed much shorter reaction times with comparable yields comparison to the corresponding thermal conditions.
