19336-97-1 Usage
Molecular structure
2-[(3-methoxyphenyl)carbamoyl]benzoic acid consists of a benzoic acid core with a carbamoyl group attached to the phenyl ring at the para position and a methoxy group at the meta position.
Organic compound
It is an organic compound, meaning it is primarily composed of carbon, hydrogen, and other elements such as oxygen and nitrogen.
Building block in synthesis
It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals, meaning it is a key component in the creation of other compounds.
Medicinal properties
The compound has been found to exhibit potential anti-inflammatory and anti-cancer properties, making it a subject of interest in medicinal chemistry research.
Enzyme inhibition
It has been identified as a potential inhibitor of the enzyme, carbonyl reductase, which is involved in the reduction of carbonyl groups.
Drug discovery and development
Its structure and properties make it a valuable tool for further exploration in drug discovery and development, meaning it has the potential to be used in the creation of new drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 19336-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,3 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19336-97:
(7*1)+(6*9)+(5*3)+(4*3)+(3*6)+(2*9)+(1*7)=131
131 % 10 = 1
So 19336-97-1 is a valid CAS Registry Number.
19336-97-1Relevant academic research and scientific papers
COMPOUNDS AND METHODS FOR INDUCING CHONDROGENESIS
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Paragraph 0739; 0876, (2014/09/29)
Described herein are compounds and compositions for the amelioration of arthritis or joint injuries by inducing mesenchymal stem cells into chondrocytes.
The cyclisation of substituted phthalanilic acids in acetic acid solution. A kinetic study of substituted N-phenylphthalimide formation
Perry, Christopher J.,Parveen, Zahida
, p. 512 - 521 (2007/10/03)
One novel and ten known substituted 3′- and 4′-phthalanilic acids have been prepared. These have been cyclised to two novel and nine known substituted N-phenylphthalimides by heating with glacial acetic acid. Both phthalanilic acids and imides have been characterised in detail and spectroscopic data are given. The kinetics of cyclisation for phthalanilic acids has been examined in detail, and it has emerged that a complex mechanism is operating. This initially involves a reversible, solvent assisted intramolecular nucleophilic attack by amide nitrogen on the carboxylic acid carbonyl. Clear evidence is seen for a long-lived intermediate as a precursor to imide formation. The observed kinetics are rationalised using a model of rapid pre-equilibration, followed by the slow breakdown of the intermediate to imide. Observed rate constants for pre-equilibration show a well behaved, linear Hammett plot (ρ = -1.1), whereas those for formation of imide do not.
