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2-([(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)amino]carbonyl)benzoic acid is a complex organic compound with the molecular formula C19H16N2O4. It is characterized by a benzoic acid core, with a pyrazole ring attached to the amino group. The pyrazole ring itself features a 1,5-dimethyl substitution, a 3-oxo group, and a 2-phenyl group, which together contribute to the compound's structure and potential applications. This chemical is known for its pharmaceutical relevance, often used as an intermediate in the synthesis of various drugs due to its ability to form stable derivatives and its potential biological activity.

19357-14-3

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19357-14-3 Usage

Molecular Structure

2-([(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)amino]carbonyl)benzoic acid is a complex organic compound that consists of a benzoic acid group, a pyrazole ring, a phenyl group, and a carbonyl group.

Benzoic Acid Group

A commonly used organic compound in various industries, the benzoic acid group is characterized by a carboxyl group (-COOH) attached to a benzene ring.

Pyrazole Ring

A five-membered aromatic ring with a nitrogen atom and two carbon atoms, the pyrazole ring can have various biological activities and is often found in bioactive compounds.

Phenyl Group

A phenyl group is a benzene ring with a hydrogen atom replaced by a functional group, which in this case is connected to the pyrazole ring.

Carbonyl Group

A carbonyl group (C=O) is a functional group consisting of a carbon atom double-bonded to an oxygen atom. In 2-([(1,5-DIMETHYL-3-OXO-2-PHENYL-2,3-DIHYDRO-1H-PYRAZOL-4-YL)AMINO]CARBONYL)BENZOIC ACID, it is present as an amide (-CONH-) and is responsible for connecting the pyrazole ring to the benzoic acid group.

Potential Applications

Due to the presence of functional groups commonly found in bioactive compounds and organic synthesis, 2-([(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)amino]carbonyl)benzoic acid may have potential pharmacological or industrial applications.

Biological Activity

The presence of the pyrazole ring suggests that 2-([(1,5-DIMETHYL-3-OXO-2-PHENYL-2,3-DIHYDRO-1H-PYRAZOL-4-YL)AMINO]CARBONYL)BENZOIC ACID may exhibit biological activity, although further research and testing would be required to determine its specific effects and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 19357-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,5 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19357-14:
(7*1)+(6*9)+(5*3)+(4*5)+(3*7)+(2*1)+(1*4)=123
123 % 10 = 3
So 19357-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C19H17N3O4/c1-12-16(18(24)22(21(12)2)13-8-4-3-5-9-13)20-17(23)14-10-6-7-11-15(14)19(25)26/h3-11H,1-2H3,(H,20,23)(H,25,26)/p-1

19357-14-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1,5-dimethyl-3-oxo-2-phenylpyrazol-4-yl)carbamoyl]benzoate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:19357-14-3 SDS

19357-14-3Relevant academic research and scientific papers

Studies on new cyclic imides obtained from aminophenazone with analgesic properties / Potent effects of a 3,4-dichloromaleimide derivative

De Campos, Fatima,Correa, Rogerio,De Souza, Marcia Maria,Yunes, Rosendo Augusto,Nunes, Ricardo Jose,Cechinel-Filho, Valdir

, p. 455 - 461 (2007/10/03)

This paper describes the synthesis of new cyclic imides obtained by reaction with aminophenazone (CAS 58-15-1, 4-aminoantipyrine) and different anhydrides with further cyclization with acetic acid under reflux. Their Structures were confirmed by spectral data (IR and NMR) and elemental analysis. The analgesic activity of the synthesized compounds was investigated initially with the writhing test in mice and the most promising compound, a 3,4-dichloromaleimide derivative (3), was analyzed using other models of nociception. The results indicated that compound 3 exerts potent analgesic activity in mice, being more active than some reference drugs. The analgesia caused by this compound was not reversed by naloxone in the writhing test. In the hotplate test, compound 3 did not increase the latency period of pain induced by thermal stimuli, confirming that it does not interact with opioid systems.

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