Nom du produit:N-[2-(azetidin-1-yl)-2-(thiophen-3-yl)ethyl]-4-(2-methyl-1,3-oxazol-4-yl)benzene-1-sulfonamide
IUPAC Name:N-[2-(azetidin-1-yl)-2-(thiophen-3-yl)ethyl]-4-(2-methyl-1,3-oxazol-4-yl)benzene-1-sulfonamide
- CAS:2034399-86-3
- Formule moléculaire:C19H21N3O3S2
- Pureté:95%+
- Numéro de catalogue:CM982391
- Poids moléculaire:403.52
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Détails du produit
- N° CAS:2034399-86-3
- Formule moléculaire:C19H21N3O3S2
- Point de fusion:-
- Code SMILES:CC1=NC(=CO1)C1=CC=C(C=C1)S(=O)(=O)NCC(N1CCC1)C1=CSC=C1
- Densité:
- Numéro de catalogue:CM982391
- Poids moléculaire:403.52
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Thiophenes
- Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
- Oxazoles
- Oxazoles are heterocyclic aromatic compounds containing one oxygen atom and one nitrogen atom, separated by a carbon atom. The presence of two heteroatoms (oxygen and nitrogen) provides possible interactions (hydrogen, hydrophobic, van der Waals or dipole bonds) with a wide range of receptors and enzymes. Oxazole rings are valuable heterocyclic scaffolds for the design of novel therapeutics with anticancer, antiviral, antibacterial, anti-inflammatory, neuroprotective, antidiabetic, and antidepressant properties due to their wide range of targets and biological activities.
- 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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