Pyridine derivatives
Pyridine derivatives contain a six-membered aromatic ring with one nitrogen atom. Substitution at the 2-, 3-, or 4-position produces distinct isomers; further substitution or ring fusion creates additional identities. Pyridine N-oxides, pyridinium salts, reduced analogues, and fused systems should be identified separately.
Published research uses defined pyridines as heteroaryl building blocks, functionalisation substrates, and ligands in coordination or catalytic systems. These roles do not imply common activity or performance. Confirm the full name, structure, CAS number where available, formula, substituent positions, and charge state. For an unlisted analogue, send an exact structure or identifier with your custom-synthesis enquiry.
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Products
N-(2-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)-2,4-difluorobenzenesulfonamide
8-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde
For 8-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde, the record confirms CAS 1232038-99-1, formula C8H5BrN2O, PubChem CID 58449869, and InChIKey UPVVPSKLFGVMEI-UHFFFAOYSA-N.
8-bromoimidazo[1,2-a]pyridine
3-Acetylaminomethyl pyridine
5-Cyano-2-Methylpyridine
6-Bromo-3-pyridinemethanol
3-chloro-5-(chloroMethyl)-pyridine
(5-Aminopyridin-2-yl)methanol
(5-Aminopyridin-2-yl)methanol, CAS 873651-92-4, has formula C6H8N2O, molecular weight 124.14, and PubChem CID 20583240.
6-Methoxynicotinamide
4-(Chloromethyl)pyridine
(3-Bromopyridin-2-yl)methanol
(3-Bromopyridin-2-yl)methanol, CAS 52378-64-0, has molecular formula C6H6BrNO and corresponds to PubChem CID 14022521.