CAS 189224-48-4
:2-(2-ETHYL-2,3-DIHYDRO-2-BENZOFURANYL)-1H-IMIDAZOLE
Description:
2-(2-Ethyl-2,3-dihydro-2-benzofuranyl)-1H-imidazole is a chemical compound characterized by its unique structure, which combines a benzofuran moiety with an imidazole ring. This compound typically exhibits properties associated with both heterocyclic compounds and aromatic systems, including potential biological activity. The presence of the imidazole ring suggests that it may participate in various chemical reactions, including coordination with metal ions and protonation, which can influence its solubility and reactivity. The ethyl group and the benzofuran structure contribute to its hydrophobic characteristics, potentially affecting its interaction with biological membranes. Additionally, compounds of this nature may exhibit pharmacological properties, making them of interest in medicinal chemistry. However, specific data regarding its solubility, melting point, and biological activity would require further investigation through experimental studies or literature review. Overall, 2-(2-ethyl-2,3-dihydro-2-benzofuranyl)-1H-imidazole represents a complex organic molecule with potential applications in various fields, including pharmaceuticals and materials science.
Formula:C13H14N2O
InChI:InChI=1/C13H14N2O/c1-2-13(12-14-7-8-15-12)9-10-5-3-4-6-11(10)16-13/h3-8H,2,9H2,1H3,(H,14,15)
SMILES:CCC1(Cc2ccccc2O1)c1ncc[nH]1
Synonyms:- Ku14R
- 2-(2-ethyl-2,3-dihydro-1-benzofuran-2-yl)-1H-imidazole
- 2-(2-ETHYL-2,3-DIHYDRO-2-BENZOFURANYL)-1H-IMIDAZOLE
- KU-14R; KU 14R
- 1H-IMidazole,2-(2-ethyl-2,3-dihydro-2-benzofuranyl)-
- 2-(2-ETHYL-2,3-DIHYDRO-2-BENZOFURANYL)-1H-IMIDAZOLE USP/EP/BP
- CS-891
- 2-(2-ethyl-3H-1-benzofuran-2-yl)-1H-imidazole
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
1H-Imidazole, 2-(2-ethyl-2,3-dihydro-2-benzofuranyl)-
CAS:Formula:C13H14N2OPurity:98%Molecular weight:214.2631KU14R
CAS:<p>KU14R is a novel molecule that can be used as a pharmacological agent to treat diabetes. It blocks the ATP-sensitive potassium channels in the hippocampus, which leads to an increase in cytosolic calcium levels and inhibits beta-cell function. KU14R also blocks the ATP-sensitive potassium channels in the bladder, which results in increased camp levels and pge2 levels. This drug has been shown to have a beneficial effect on diabetic patients. The molecular targets of KU14R are intracellular targets including transcription-polymerase chain and protein synthesis. KU14R also inhibits potassium channel activity by blocking voltage-gated potassium channels, leading to an increase in cytosolic calcium levels and inhibition of beta-cell function.</p>Formula:C13H14N2OPurity:Min. 95%Molecular weight:214.27 g/molKU14R
CAS:<p>KU14R is a new I(3)-R antagonist, which selectively blocks the insulin secretory response to imidazolines.</p>Formula:C13H14N2OPurity:98%Color and Shape:White SolidMolecular weight:214.26




