Nom du produit:3-(1H-Benzo[d]imidazol-2-yl)-7-(diethylamino)-2H-chromen-2-one
IUPAC Name:3-(1H-1,3-benzodiazol-2-yl)-7-(diethylamino)-2H-chromen-2-one
- CAS：27425-55-4
- Formule moléculaire：C20H19N3O2
- Pureté：95%
- Numéro de catalogue：CM161929
- Poids moléculaire：333.39
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:27425-55-4
- Formule moléculaire:C20H19N3O2
- Point de fusion:-
- Code SMILES:O=C1C(C2=NC3=CC=CC=C3N2)=CC4=C(O1)C=C(N(CC)CC)C=C4
- Densité:
- Numéro de catalogue:CM161929
- Poids moléculaire:333.39
- Point d'ébullition:
- N° Mdl:MFCD00051348
- Stockage:
Category Infos
- Benzimidazoles
- Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.
- Coumarins
- Coumarin occurs naturally in a variety of plants, such as lentils, sweet sawdust, vanilla grass, and sweet grass. Coumarin has a simple structure, benzopyrone, associated with different reaction centers. Coumarins are further subdivided into different classes: simple coumarins, pyranocoumarins, furanocoumarins, dicoumarins and isocoumarins. Coumarin derivatives are an important class of natural plant metabolites with various biological activities. They can also be synthesized artificially, and various synthetic coumarin derivatives (azoles, sulfonyls, furans, pyrazoles, etc.) have shown good anticancer, antitumor and antiproliferative activities. Coumarin derivatives are not only effective anticancer agents, but also possess minimum side effects. Based on different substitution patterns, these potential active substances show a great ability to modulate potential anticancer activities.
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