Nom du produit:1-(4-methoxy-1,3-benzothiazol-2-yl)azetidin-3-yl 3-(2,5-dioxopyrrolidin-1-yl)benzoate
IUPAC Name:1-(4-methoxy-1,3-benzothiazol-2-yl)azetidin-3-yl 3-(2,5-dioxopyrrolidin-1-yl)benzoate
- CAS:1421531-09-0
- Formule moléculaire:C22H19N3O5S
- Pureté:95%+
- Numéro de catalogue:CM793014
- Poids moléculaire:437.47
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1421531-09-0
- Formule moléculaire:C22H19N3O5S
- Point de fusion:-
- Code SMILES:COC1=C2N=C(SC2=CC=C1)N1CC(C1)OC(=O)C1=CC(=CC=C1)N1C(=O)CCC1=O
- Densité:
- Numéro de catalogue:CM793014
- Poids moléculaire:437.47
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Pyrrolidines
- Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.
- Benzothiazoles
- Benzothiazoles are aromatic heterocyclic compounds with the chemical formula C7H5NS. Benzothiazoles and their derivatives are a very important class of heterocyclic compounds that are ubiquitous in nature and are mainly used in medicine, agriculture and industry. In medicine, benzothiazole derivatives are a kind of very important pharmaceutical intermediates with good pharmacological and biological activities. It can be used as a fungicide, anti-tuberculosis drug, anti-malarial, anti-convulsant, insecticide, sedative and anti-inflammatory drug, and can also be used to treat diabetes and has anti-cancer effects.
- 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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