Nombre del producto:(R)-2-methylpropane-2-sulfinamide

IUPAC Name:(R)-2-methylpropane-2-sulfinamide

CAS:196929-78-9
Fórmula molecular:C4H11NOS
Pureza:99%
Número de catálogo:CM112195
Peso molecular:121.2

Unidad de embalaje Stock disponible Precio($) Cantidad
CM112195-200g in stock Ƥdž

Sólo para uso en I+D..

Formulario de consulta

   refresh    

Detalles del producto

Núm. De CAS :196929-78-9
Fórmula molecular:C4H11NOS
Punto de fusión:-
Código de sonrisas:CC([S@](N)=O)(C)C
Densidad:
Número de catálogo:CM112195
Peso molecular:121.2
Punto de ebullición:
Nº Mdl:MFCD05861479
Almacenamiento:Keep in a tight container and store at 2°C~8°C

Column Infos

Nitrogen Compounds
Nitrogen compounds can be classified as mineral or organic. Mineral compounds are essentially formed by the ammonium ion (NH4+), which is generated when ammonium salts are dissolved in water. Organic compounds, in contrast, are carbon and hydrogen compounds that contain a nitrogen atom. All organic nitrogen-containing compounds can be considered as derivatives of ammonia in which one or more hydrogen atoms are substituted by hydrocarbon radicals.
Repotrectinib
Repotrectinib receives approval for the treatment of adult patients with locally advanced or metastatic ROS1-positive non-small cell lung cancer (NSCLC) from the U.S. FDA on November 15, 2023. ROS1 gene is altered in about 1-2% of patients with NSCLC. ROS1-positive lung cancer tends to be aggressive and can spread to the brain and the bones.
Repotrectinib is a highly potent and differentiated small molecule TKI that binds inside the ATP pocket, and is active against both wild-type and resistant mutations, including solvent front and gatekeeper mutations. Repotrectinib is expected to enter the U.S. market in mid-December 2023.
Olutasidenib
Rigel announces publication of data on REZLIDHIA(Olutasidenib) in post-venetoclax patients with mutant IDH1 AML in Leukemia & Lymphoma.
REZLIDHIA (Olutasidenib), a potent, selective, oral, small-molecule inhibitor of mutant isocitrate dehydrogenase-1 (mIDH1), in patients with mIDH1 acute myeloid leukemia (AML) who were relapsed/refractory (R/R) to prior venetoclax-based regimens.