Produktname:(5-methyl-2-oxo-1,3-dioxol-4-yl)methyl (5R,6S)-6-((R)-1-hydroxyethyl)-7-oxo-3-((R)-tetrahydrofuran-2-yl)-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
IUPAC Name:(5-methyl-2-oxo-2H-1,3-dioxol-4-yl)methyl (5R,6S)-6-[(1R)-1-hydroxyethyl]-7-oxo-3-[(2R)-oxolan-2-yl]-4-thia-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate
- CAS:141702-36-5
- Molekulare Formel:C17H19NO8S
- Reinheit:98%
- Katalognummer:CM195914
- Molekulargewicht:397.4
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Produkt-Details
- CAS-Nr.:141702-36-5
- Molekulare Formel:C17H19NO8S
- Schmelzpunkt:-
- SMILES-Code:O=C(C(N12)=C([C@@H]3OCCC3)S[C@]2([H])[C@@H]([C@H](O)C)C1=O)OCC4=C(C)OC(O4)=O
- Dichte:
- Katalognummer:CM195914
- Molekulargewicht:397.4
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- 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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- Tetrahydrofurans
- Tetrahydrofuran is a heterocyclic organic compound with the molecular formula C4H8O. Tetrahydrofuran belongs to ethers and is the complete hydrogenation product of furan. It is a colorless, water-miscible organic liquid with small viscosity at normal temperature and pressure. Because of its long liquid range, it is a commonly used medium polar aprotic solvent. Its main use is as a precursor of high molecular polymers.
- Thiazolines
- Thiazolines are a group of isomeric five-membered heterocyclic compounds containing both sulfur and nitrogen. Thiazoline exists in three isomeric forms namely 2-thiazoline, 3-thiazoline and 4-thiazoline. Oxazolines, oxazoles, thiazolines, and thiazoles form the characteristic heterocyclic building blocks of lissoclinum peptide alkaloids.