19652-14-3 Usage
Description
5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE is an organic compound with the molecular formula C15H11ClN3. It is characterized by its pyrazol-3-ylamine structure, which is a derivative of pyrazole, a five-membered heterocyclic compound. The presence of a chlorophenyl and phenyl group in the molecule contributes to its chemical properties and potential applications.
Uses
Used in Pharmaceutical Industry:
5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE is used as a reactant in the preparation of trifluoromethyl-substituted pyrazolo[3,4-b]pyridines. These compounds are of interest due to their antimicrobial properties, making them potentially useful in the development of new drugs to combat various types of infections.
Used in Chemical Synthesis:
In the field of chemical synthesis, 5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE can serve as a building block or intermediate for the creation of more complex molecules with diverse applications. Its unique structure allows for further functionalization and modification, which can lead to the development of new compounds with specific properties and uses.
Used in Research and Development:
Due to its structural features, 5-(4-CHLORO-PHENYL)-2-PHENYL-2H-PYRAZOL-3-YLAMINE may be utilized in research and development for various purposes, such as studying its chemical reactivity, exploring its potential as a precursor to other compounds, or investigating its biological activities. This can contribute to the advancement of knowledge in the fields of chemistry, biology, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 19652-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,6,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19652-14:
(7*1)+(6*9)+(5*6)+(4*5)+(3*2)+(2*1)+(1*4)=123
123 % 10 = 3
So 19652-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H12ClN3/c16-12-8-6-11(7-9-12)14-10-15(17)19(18-14)13-4-2-1-3-5-13/h1-10H,17H2
19652-14-3Relevant articles and documents
Highly Efficient Chemoselective Synthesis of Pyrrolo[2,3- c ]pyrazole Bearing Oxindole via Sequential Condensation-Michael Addition-Intramolecular Cyclization Reactions
Farhid, Hassan,Javanbakht, Siamak,Nazeri, Mohammad Taghi,Notash, Behrouz,Shaabani, Ahmad
, p. 965 - 971 (2020)
An efficient and highly chemoselective approach for the synthesis of novel scaffolds based on pyrrolo[2,3- c ]pyrazole bearing oxindole is accomplished by the acid-promoted sequential reactions between benzoylacetonitriles, phenylhydrazine, and 3-phenacyl
Phenyl pyrazole compound, pharmaceutical composition and preparation method and application of phenyl pyrazole compound
-
Paragraph 0520-0522, (2020/02/19)
The invention discloses a phenyl pyrazole compound, a pharmaceutical composition and a preparation method and application of the phenyl pyrazole compound. The phenyl pyrazole compound shown in a formula I or a formula II can be used for preparing drugs fo
"On-Water" Facile Synthesis of Novel Pyrazolo[3,4-b]pyridinones Possessing Anti-influenza Virus Activity
Zeng, Li-Yan,Liu, Teng,Yang, Jie,Yang, Yueli,Cai, Chun,Liu, Shuwen
supporting information, p. 437 - 446 (2017/07/15)
A facile and versatile "on-water" protocol for the synthesis of pyrazolo[3,4-b]pyridinones was developed by the unprecedented construction of two rings and five new bonds in one-pot. It was proved that water was an important promoter of the reaction and P
