Название продукции:methyl 3-({3-[(4-methoxy-1,3-benzothiazol-2-yl)oxy]azetidin-1-yl}sulfonyl)thiophene-2-carboxylate

IUPAC Name:methyl 3-({3-[(4-methoxy-1,3-benzothiazol-2-yl)oxy]azetidin-1-yl}sulfonyl)thiophene-2-carboxylate

CAS:1421451-97-9
Молекулярная формула:C17H16N2O6S3
Чистота:95%+
Номер в каталоге:CM923944
Молекулярная масса:440.5

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Информация о продукции

Номер CAS:1421451-97-9
Молекулярная формула:C17H16N2O6S3
Точка плавления:-
Smiles-код:COC(=O)C1=C(C=CS1)S(=O)(=O)N1CC(C1)OC1=NC2=C(OC)C=CC=C2S1
Плотность:
Номер в каталоге:CM923944
Молекулярная масса:440.5
Точка кипения:
Номер Mdl:
Хранение:

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.
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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