1-(4-((3-chloro-4-((6-methylpyridin-3-yl)oxy)phenyl)amino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)prop-2-en-1-one

1-(4-((3-chloro-4-((6-methylpyridin-3-yl)oxy)phenyl)amino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)prop-2-en-1-one

4-amino-5-(6-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)thieno[2,3-b]pyridin-6(7H)-one (2S,3S)-2,3-dihydroxysuccinate

4-amino-5-(6-(4-methylpiperazin-1-yl)-1H-benzo[d]imidazol-2-yl)thieno[2,3-b]pyridin-6(7H)-one (2S,3S)-2,3-dihydroxysuccinate

N-(6-methylpyridin-2-yl)-4-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)-3-(3-(trifluoromethyl)benzamido)benzamide

$360.00
CAS No.: 441050-81-3
Catalog No.: 198539
Purity: 95%
MF: C32H28F3N5O3
MW: 587.602
Storage: 2-8 degree Celsius
SMILES: CC1=CC=CC(=N1)NC(C1=CC(=C(C=C1)N1CC2C=3N(CC(C1)C2)C(C=CC3)=O)NC(C3=CC(=CC=C3)C(F)(F)F)=O)=O
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CAS No.:441050-81-3;N-(6-methylpyridin-2-yl)-4-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)-3-(3-(trifluoromethyl)benzamido)benzamide;As a premier chemical synthesis company specializing in complex heterocyclic compounds and amide derivatives, ChemShuttle offers the N-(6-methylpyridin-2-yl)-4-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)-3-(3-(trifluoromethyl)benzamido)benzamide (CAS No.:441050-81-3). This compound represents a sophisticated building block designed for advanced applications in drug discovery and development. The molecule integrates a benzamide core with multiple pharmacophores, including a pyridinyl group, a diazocin ring system with an oxo group, and a trifluoromethyl-substituted benzamido group. Such a combination creates a versatile platform for further functionalization and target engagement in medicinal chemistry. As a worldwide chemical supplier, we ensure the availability of this specialized intermediate to support researchers in their quest for novel therapeutic agents. Our custom synthesis services can modify this compound to incorporate additional functionalities or adjust existing ones, enhancing its utility as a key intermediate. The strategic placement of the amide bonds, the heterocyclic rings, and the trifluoromethyl substituent provides numerous points for chemical modification. This allows for the creation of diverse libraries of compounds for biological screening and medicinal chemistry applications.

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