Nombre del producto:(1R,2R,4S,5S)-3,9-dioxatricyclo[3.3.1.02,4]nonan-7-one

IUPAC Name:(1R,2R,4S,5S)-3,9-dioxatricyclo[3.3.1.0²,⁴]nonan-7-one

CAS:99892-53-2
Fórmula molecular:C7H8O3
Pureza:95%+
Número de catálogo:CM542627
Peso molecular:140.14

Unidad de embalaje Stock disponible Precio($) Cantidad
CM542627-100mg 1-2 Weeks ŭƩƻş

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :99892-53-2
Fórmula molecular:C7H8O3
Punto de fusión:-
Código de sonrisas:O=C1C[C@@]2([H])[C@]3([H])O[C@]3([H])[C@@](O2)([H])C1
Densidad:
Número de catálogo:CM542627
Peso molecular:140.14
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Oxiranes
Oxirane is a three-membered ring compound consisting of one oxygen atom and two carbon atoms. Oxirane is present in natural products such as cryptocin, which has anticancer properties, and azidomycin, trienone, and epoxidomycin, which have shown activity against drug-resistant leukemias and AIDS-related lymphomas. Other oxirane containing bioactive molecules have anti-inflammatory, immunosuppressive, and antitumor activities. Oxiranes are a strained ring susceptible to various nucleophilic, ring-opening or rearrangement reactions, so they are considered to be one of the most important intermediates in organic synthesis.
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.
Tetrahydropyrans
Tetrahydropyran is an organic compound consisting of a saturated six-membered ring containing five carbon atoms and one oxygen atom. Tetrahydropyrans are common structural motifs in natural products and synthetic therapeutic molecules. In nature, these six-membered oxygen heterocycles are usually assembled by intramolecular reactions, including oxygen Michael addition or ring opening of epoxy alcohols. In fact, polyether natural products have been particularly extensively studied for their fascinating structures and important biological properties; these are often formed through endoselective epoxy open cascades.