99552-32-6 Usage
Description
N-(2,4-dimethylphenyl)piperidine-2-carboxamide is a synthetic compound characterized by the chemical formula C16H24N2O. It is a derivative of piperidine, featuring a carboxamide group and a 2,4-dimethylphenyl substituent. N-(2,4-dimethylphenyl)piperidine-2-carboxamide is recognized for its potential to engage with biological systems, making it a valuable entity in the realms of pharmacology and medicinal chemistry. Its utility extends beyond mere research, as it serves as a chemical building block or intermediate in the synthesis of other compounds. However, due to its potential hazards if mishandled, careful use is warranted.
Uses
Used in Laboratory Research:
N-(2,4-dimethylphenyl)piperidine-2-carboxamide is utilized as a chemical building block or intermediate for the synthesis of other compounds, playing a crucial role in advancing scientific studies and the development of new chemical entities.
Used in Pharmacology and Medicinal Chemistry:
In the field of pharmacology and medicinal chemistry, N-(2,4-dimethylphenyl)piperidine-2-carboxamide is employed for its capacity to interact with biological systems, which positions it as a promising candidate for the creation of novel therapeutic agents.
Used in Chemical Synthesis:
N-(2,4-dimethylphenyl)piperidine-2-carboxamide is used as a key intermediate in the synthesis of a variety of chemical products, contributing to the diversification of chemical libraries and the discovery of new molecules with potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 99552-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,5,5 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 99552-32:
(7*9)+(6*9)+(5*5)+(4*5)+(3*2)+(2*3)+(1*2)=176
176 % 10 = 6
So 99552-32-6 is a valid CAS Registry Number.
99552-32-6Relevant articles and documents
Synthesis, Characterization and Biological Evaluation of Some Novel Regioisomers of Ropivacaine Analogues: An Anaesthetic Drug
Sharavanan,Venkatesan,Bhaskara Suresh Raju,Kabilan
, p. 2180 - 2186 (2020/09/16)
A series of ropivacaine analogues were synthesized by altering the methyl group substituent in the aromatic ring. The synthesized compounds (2a-f and 3a-f) were characterized by using IR, NMR and HRMS analysis and then compounds 3a-3f were screened in vitro anticancer (MTT assay) activity against breast cancer cell line (MCF-7), antibacterial and antioxidant (DPPH scavenging assay) studies. The biological studies revealed that the compounds 3c and 3f have shown a good inhibitory activity against MCF-7 cell line. Compounds 3e, 3b, 3c and 3f showed moderate antioxidant activity. There was no inhibition observed against both Gram-positive and Gram-negative bacteria.
