905307-07-5 Usage
Vinyl derivative of pyrazole
The compound is derived from pyrazole, a five-membered heterocyclic ring, by attaching a vinyl group (a carbon-carbon double bond) to its structure. This modification introduces new reactivity and properties to the molecule.
Carboxylic acid functional group
The presence of a carboxylic acid group (-COOH) in the molecule grants it acidic properties and allows for the formation of hydrogen bonds, which can influence its solubility, stability, and reactivity in various chemical reactions.
Building block in organic synthesis
The compound can be used as a building block to create a variety of heterocyclic compounds, which are valuable in the development of new drugs, agrochemicals, and other applications.
Ligand in coordination chemistry
1-vinyl-1H-pyrazole-4-carboxylic acid has the potential to act as a ligand, a molecule that can donate a pair of electrons to a metal ion, in coordination chemistry. This property allows it to form complexes with metal ions, which may have interesting properties or applications.
Biological activity
The compound may exhibit biological activity in certain applications, such as acting as an enzyme inhibitor, receptor agonist/antagonist, or having antimicrobial properties. This makes it a potentially valuable molecule for the development of new drugs and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 905307-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,3,0 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 905307-07:
(8*9)+(7*0)+(6*5)+(5*3)+(4*0)+(3*7)+(2*0)+(1*7)=145
145 % 10 = 5
So 905307-07-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N2O2/c1-2-8-4-5(3-7-8)6(9)10/h2-4H,1H2,(H,9,10)
905307-07-5Relevant academic research and scientific papers
Synthesis of 1-vinyl-4-pyrazolecarboxylic acids
Baltayan,Saakyan,Attaryan,Asratyan
, p. 1004 - 1006 (2011/01/05)
A convenient oxidation method of 1-(2-chloroethyl)-4-formylpyrazoles followed by dehydrochlorination was developed for preparation of 1-vinyl-4-pyrazolecarboxylic acids. Dehydrochlorination rate was established to decrease with the growing number of electron-donor substituents. Pleiades Publishing, Ltd., 2010.
OPTICALLY ACTIVE TETRAHYDRONAPHTHALENE DERIVATIVE
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Page/Page column 18, (2010/11/28)
A compound represented by the following formula (I), a pharmacologically acceptable salt thereof or a hydrate thereof or a solvate thereof, which shows not only a C5a receptor antagonistic activity but also high activity in the biological availability, as
