CAS 676266-31-2
:N-[2-Methyl-5-phenyl-3-[[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]methyl]-1H-pyrrol-1-yl]-4-pyridinecarboxamide
Description:
N-[2-Methyl-5-phenyl-3-[[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]methyl]-1H-pyrrol-1-yl]-4-pyridinecarboxamide, with CAS number 676266-31-2, is a synthetic organic compound characterized by its complex molecular structure, which includes multiple functional groups such as a pyridinecarboxamide and a piperazine moiety. This compound typically exhibits properties associated with its aromatic and heterocyclic components, including potential lipophilicity and the ability to engage in hydrogen bonding due to the presence of amide functionalities. It may also display biological activity, making it of interest in pharmaceutical research, particularly in the development of therapeutic agents. The trifluoromethyl group enhances its electronic properties, potentially influencing its interaction with biological targets. As with many compounds of this nature, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other substances. Safety and handling precautions are essential when working with this compound, as it may possess toxicological properties that require careful assessment.
Formula:C29H28F3N5O
InChI:InChI=1S/C29H28F3N5O/c1-21-24(20-35-14-16-36(17-15-35)26-9-5-8-25(19-26)29(30,31)32)18-27(22-6-3-2-4-7-22)37(21)34-28(38)23-10-12-33-13-11-23/h2-13,18-19H,14-17,20H2,1H3,(H,34,38)
InChI key:InChIKey=PRXZOPNJRFEGRH-UHFFFAOYSA-N
SMILES:N(C(=O)C=1C=CN=CC1)N2C(=CC(CN3CCN(CC3)C4=CC(C(F)(F)F)=CC=C4)=C2C)C5=CC=CC=C5
Synonyms:- 4-Pyridinecarboxamide, N-[2-methyl-5-phenyl-3-[[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]methyl]-1H-pyrrol-1-yl]-
- N-[2-Methyl-5-phenyl-3-[[4-[3-(trifluoromethyl)phenyl]-1-piperazinyl]methyl]-1H-pyrrol-1-yl]-4-pyridinecarboxamide
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Found 3 products.
Sudoterb free
CAS:<p>Sudoterb free is a pyridine compound that has been shown to be active against resistant infections. This drug has been clinically used for the treatment of asymptomatic infection, and is in clinical development for the treatment of tuberculosis. The trifluoromethyl group on the pyridine ring is responsible for its anti-tuberculosis effects. Sudoterb free has been shown to have a pharmacokinetic profile that is tissue-specific and differs from other drugs in its class. It also has multidrug resistance, which may be due to its quinoline derivatives (quinolones).</p>Formula:C29H28F3N5OPurity:Min. 95%Molecular weight:519.6 g/molSudoterb free base
CAS:Sudoterb free base (Sudoterb) , also known as LL3858, is an anti-tubercular drug candidate.Formula:C29H28F3N5OPurity:97.26% - 98.85%Color and Shape:SolidMolecular weight:519.56


