![2-(4-Nitrophenyl)imidazo[1,2-a]pyridine](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F119772-2-4-nitrophenyl-imidazo-12-a-pyridine.webp&w=3840&q=75)
CAS 3323-26-0: 2-(4-Nitrophenyl)imidazo[1,2-a]pyridine
Formula:C13H9N3O2
InChI:InChI=1S/C13H9N3O2/c17-16(18)11-6-4-10(5-7-11)12-9-15-8-2-1-3-13(15)14-12/h1-9H
InChI key:InChIKey=SNBCSKCONKUZBA-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC=C(C2=CN3C(=N2)C=CC=C3)C=C1
Synonyms:- 2-(4-Nitro-phenyl)-imidazo[1,2-a]pyridine
- Imidazo[1,2-a]pyridine, 2-(4-nitrophenyl)-
- Imidazo[1,2-a]pyridine, 2-(p-nitrophenyl)-
- 2-(4-Nitrophenyl)imidazo[1,2-a]pyridine
Sort by
Found 4 products.
2-(4-Nitrophenyl)imidazo[1,2-a]pyridine
CAS:2-(4-Nitrophenyl)imidazo[1,2-a]pyridineColor and Shape:SolidMolecular weight:239.23g/mol2-(4-Nitrophenyl)imidazo[1,2-a]pyridine
CAS:2-(4-Nitrophenyl)imidazo[1,2-a]pyridine (NPI) is an orally active fluorescent probe for angiotensin II receptor type 1 (AT1). The fluorescence of NPI is quenched in the presence of AT1. Under conditions with high concentrations of AT1, the fluorescence of NPI changes from green to red. This property allows the measurement of AT1 levels in cells and tissues. In addition, NPI is a substrate for phenacyl choline esterase that catalyzes the hydrolysis of 2-(4-nitrophenyl)-imidazo[1,2-a]pyridine to 2-(4-nitrophenyl)-3-hydroxypyridine. The reaction time and temperature are dependent on the substrate concentration as well as pH and ionic strength. Reaction times increase with decreasing pH and increasing ionic strength.Formula:C13H9N3O2Purity:Min. 95%Molecular weight:239.23 g/molRef: 3D-FN131943
Discontinued product8-(4-nitrophenyl)-1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraene
CAS:Formula:C13H9N3O2Purity:85%Molecular weight:239.2295