Nom du produit:3,3-difluorocyclobutane-1-carbonitrile

IUPAC Name:3,3-difluorocyclobutane-1-carbonitrile

CAS:86770-80-1
Formule moléculaire:C5H5F2N
Pureté:95%+
Numéro de catalogue:CM108791
Poids moléculaire:117.1

Unité d'emballage Stock disponible Prix($) Quantité
CM108791-10g in stock ĽƓŹ
CM108791-25g in stock ŗNJǵĽ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:86770-80-1
Formule moléculaire:C5H5F2N
Point de fusion:-
Code SMILES:N#CC1CC(F)(F)C1
Densité:
Numéro de catalogue:CM108791
Poids moléculaire:117.1
Point d'ébullition:
N° Mdl:MFCD10001482
Stockage:Store at 2-8°C.

Category Infos

Cyclobutanes
The molecular structure of cyclobutane has four carbon atoms, and its four carbon atoms are not in the same plane, which is the folded conformation of cyclobutane. Cyclobutane itself is not of commercial or biological interest, but more complex derivatives are important in biology and biotechnology. Currently, nine FDA-approved drugs contain the cyclobutane structure. From the perspective of therapeutic areas, cyclobutyl drugs are mainly distributed in popular areas such as tumors, neurological diseases, infectious diseases, endocrine and metabolic diseases.

Column Infos

Cyclanes
Cyclanes are secondary metabolites that can be found in plants, and are also biochemicals that can be used in medicine. Cyclanes are found in pine trees, and are used in the making of plastics. Cyclenes are found in cinnamon, and have antifungal properties.
Fluorinated compounds
Fluorinated compounds refers to organic or inorganic compounds containing fluorine.
Ivosidenib
Tibsovo (ivosidenib tablets) is a precision medicine that targets a specific type of mutation known as isocitrate dehydrogenase 1 (IDH1). Tibsovo is approved in five indications globally, including approvals in the U.S., European Union, Australia, and China.
Tibsovo is the first and only approved targeted therapy for R/R MDS patients with a susceptible IDH1 mutation.
Fifth approved indication for Tibsovo solidifies Servier’s leadership in mutant IDH inhibition.