2,2'-Bi(1,8-naphthyridine)

Catalog Number	ACM69110334
CAS	69110-33-4
Structure
Description	2,2'-Bi(1,8-naphthyridine) is an aromatic heterocyclic compound belonging to the class of naphthyridines. It is a cyclic compound composed of two nitrogen atoms and three carbon atoms, and is a member of the biaryl family. Its chemical formula is C10H8N2. It is an important building block for the synthesis of a variety of pharmaceuticals and other organic compounds.
Synonyms	2-(1,8-Naphthyridin-2-yl)-1,8-naphthyridine
IUPAC Name	2-(1,8-naphthyridin-2-yl)-1,8-naphthyridine
Molecular Weight	258.28 g/mol
Molecular Formula	C16H10N4
Canonical SMILES	C1=CC2=C(N=C1)N=C(C=C2)C3=NC4=C(C=CC=N4)C=C3
InChI	InChI=1S/C16H10N4/c1-3-11-5-7-13(19-15(11)17-9-1)14-8-6-12-4-2-10-18-16(12)20-14/h1-10H
InChI Key	OGSULPWGXWPZOJ-UHFFFAOYSA-N
Purity	95%
Appearance	Powder or crystal
Application	2,2'-Bi(1,8-naphthyridine) has a wide range of applications in scientific research. It is used in the synthesis of a variety of pharmaceuticals, including antifungal agents, anti-inflammatory agents, and antiviral agents. It is also used in the synthesis of a variety of organic compounds, such as dyes, pigments, and other materials. In addition, it is used in the synthesis of a variety of catalysts, including those used in the production of polymers.
Complexity	302
Covalently-Bonded Unit Count	1
Exact Mass	258.091g/mol
Heavy Atom Count	20
Monoisotopic Mass	258.091g/mol
Properties	2,2'-Bi(1,8-naphthyridine) has a variety of biochemical and physiological effects. It has been found to have an inhibitory effect on monoamine oxidase, an enzyme involved in the breakdown of neurotransmitters. It has also been found to have an inhibitory effect on the activity of cytochrome P450 enzymes, which are involved in the metabolism of drugs and other xenobiotics. In addition, it has been found to have an inhibitory effect on the activity of protein kinases, enzymes involved in signal transduction pathways.
Rotatable Bond Count	1
Topological Polar Surface Area	51.6A^2