Nom du produit:6-(3-{3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-5-yl}azetidine-1-carbonyl)-1H-indole
IUPAC Name:6-(3-{3-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-5-yl}azetidine-1-carbonyl)-1H-indole
- CAS:1428348-02-0
- Formule moléculaire:C21H15F3N4O2
- Pureté:95%+
- Numéro de catalogue:CM902757
- Poids moléculaire:412.37
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1428348-02-0
- Formule moléculaire:C21H15F3N4O2
- Point de fusion:-
- Code SMILES:FC(F)(F)C1=CC=CC(=C1)C1=NOC(=N1)C1CN(C1)C(=O)C1=CC2=C(C=CN2)C=C1
- Densité:
- Numéro de catalogue:CM902757
- Poids moléculaire:412.37
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Indoles
- Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.
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- Oxadiazoles
- Oxadiazoles are a class of heterocyclic aromatic compounds with the molecular formula C2H2N2O, which have special biological activities and thermodynamic properties. Five-membered heterocyclic moieties composed of three or two heteroatoms are of great interest to researchers because these compounds show significant therapeutic potential. These heterocycles can serve as a building block for the development of novel molecular structures.
- Azetidines
- Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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