Nombre del producto:oxetan-3-one

IUPAC Name:oxetan-3-one

CAS:6704-31-0
Fórmula molecular:C3H4O2
Pureza:95%+
Número de catálogo:CM104041
Peso molecular:72.06

Unidad de embalaje Stock disponible Precio($) Cantidad
CM104041-100g in stock ƥŗŹ
CM104041-500g in stock ůŹƥ
CM104041-1000g in stock ǤNJŗ

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :6704-31-0
Fórmula molecular:C3H4O2
Punto de fusión:-
Código de sonrisas:O=C1COC1
Densidad:
Número de catálogo:CM104041
Peso molecular:72.06
Punto de ebullición:
Nº Mdl:MFCD09263255
Almacenamiento:

Category Infos

Oxetanes
Oxygen heterocycles are one of the most common heterocycles in drugs and natural products. Oxetene has high polarity and is also a good acceptor for hydrogen bond, which contributes to the metabolism and chemical stability of its host molecules. When substituted for commonly used functional groups such as gem dimethyl or carbonyl, oxetane units can induce profound changes in water solubility, lipophilicity, metabolic stability and conformational preference. Four of the FDA-approved drugs contain oxetenes: Orlistat, Paclitaxel, and two of its derivatives, Docetaxel and Cabazitaxel. Currently, oxetane-containing building blocks are flourishing in medicinal chemistry and drug discovery.

Column Infos

Alicyclic Heterocycles
When the ends of the chains are joined together into a ring, cyclic compounds result; such substances often are referred to as carbocyclic or alicyclic compounds. Substitution of one or more of the ring carbon atoms in the molecules of a carbocyclic compound with a heteroatom gives a heterocyclic compound.
Fenebrutinib
Roche’s investigational drug, Fenebrutinib has shown brain penetration and significant reduction in lesions in patients with relapsing multiple sclerosis (MS) from the recent release of new data from Phase II FENopta study. Fenebrutinib is a potent and highly selective Bruton’s tyrosine kinase (BTK) inhibitor, and currently the only reversible inhibitor being tested in Phase III MS trials. BTK inhibitor is involved in key pathological features of MS, including B-cell development and activation.

Related Products