Description
2,4-dimethoxy-N-(3-(thiazolo[5,4-b]pyridin-2-yl)phenyl)benzamide (CAS No. 863589-44-0) is a high-purity synthetic organic compound with the molecular formula C21H17N3O3S. This benzamide derivative features a thiazolo[5,4-b]pyridine core, offering unique structural and electronic properties for advanced research applications. With a molecular weight of 391.45 g/mol, this compound is characterized by its two methoxy substituents on the benzamide ring, enhancing its solubility and reactivity profile. Ideal for pharmaceutical research, medicinal chemistry, and biochemical studies, this compound is supplied with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry environment under inert conditions to maintain stability.
Properties
- CAS Number: 863589-44-0
- Complexity: 537
- IUPAC Name: 2,4-dimethoxy-N-(3-thiazolo[5,4-b]pyridin-2-ylphenyl)benzamide
- InChI: InChI=1S/C21H17N3O3S/c1-26-15-8-9-16(18(12-15)27-2)19(25)23-14-6-3-5-13(11-14)20-24-17-7-4-10-22-21(17)28-20/h3-12H,1-2H3,(H,23,25)
- InChI Key: OOLNKALQNLNRAA-UHFFFAOYSA-N
- Exact Mass: 391.09906259
- Molecular Formula: C21H17N3O3S
- Molecular Weight: 391.4
- SMILES: COC1=CC(=C(C=C1)C(=O)NC2=CC=CC(=C2)C3=NC4=C(S3)N=CC=C4)OC
- Topological: 102
- Monoisotopic Mass: 391.09906259
- Synonyms: 863589-44-0, 2,4-dimethoxy-N-(3-(thiazolo[5,4-b]pyridin-2-yl)phenyl)benzamide, 2,4-DIMETHOXY-N-(3-{[1,3]THIAZOLO[5,4-B]PYRIDIN-2-YL}PHENYL)BENZAMIDE, WAY-339500, 2,4-dimethoxy-N-[3-([1,3]thiazolo[5,4-b]pyridin-2-yl)phenyl]benzamide, (Z)-2,4-dimethoxy-N-(3-{[1,3]thiazolo[5,4-b]pyridin-2-yl}phenyl)benzene-1-carboximidic acid, SCHEMBL2740046, AKOS001900303, AS-88278, F0694-0161
Application
2,4-dimethoxy-N-(3-(thiazolo[5,4-b]pyridin-2-yl)phenyl)benzamide is a valuable intermediate in the synthesis of novel heterocyclic compounds for drug discovery. Its thiazolopyridine scaffold is of interest in the development of kinase inhibitors and other therapeutic agents targeting metabolic and inflammatory pathways. Researchers utilize this compound in structure-activity relationship (SAR) studies to optimize pharmacological properties. It may also serve as a fluorescent probe or ligand in biochemical assays due to its conjugated aromatic system.
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