cas 117548-22-8|| where to buy 2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-5-carboxylate compound with 2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-6-carboxylate (1:1)

Nom du produit:2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-5-carboxylate compound with 2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthene]-6-carboxylate (1:1)

IUPAC Name:2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[2-benzofuran-1,9'-xanthene]-5-carboxylate; 2,5-dioxopyrrolidin-1-yl 3',6'-dihydroxy-3-oxo-3H-spiro[2-benzofuran-1,9'-xanthene]-6-carboxylate

: CAS：117548-22-8; Formule moléculaire：C50H30N2O18; Pureté：97%

: Numéro de catalogue：CM139274; Poids moléculaire：946.79

Unité d'emballage	Stock disponible	Prix($)
CM139274-50mg	1-2 Weeks	Ǒƴ
CM139274-100mg	3-4 Weeks	ƴƴǫ
CM139274-500mg	4-5 Weeks	ǫȖǫ

Demande: sales@chemenu.com

Pour une utilisation en R&D uniquement..

Formulaire de demande

Nom chimique

Numéro CAS

Quantité*

Spécifications requises*
(% d'analyse, qualité du matériau, etc.)

Nom du contact*

Email du contact*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 117548-22-8 regularly via the above email.

Notes supplémentaires

Verification code*

refresh

Détails du produit

: N° CAS:117548-22-8; Formule moléculaire:C50H30N2O18; Point de fusion:-; Code SMILES:O=C(C1=CC2=C(C3(C4=C(OC5=C3C=CC(O)=C5)C=C(O)C=C4)OC2=O)C=C1)ON6C(CCC6=O)=O.O=C(C7=CC(C8(C9=C(OC%10=C8C=CC(O)=C%10)C=C(O)C=C9)O%11)=C(C=C7)C%11=O)ON%12C(CCC%12=O)=O; Densité:

: Numéro de catalogue:CM139274; Poids moléculaire:946.79; Point d'ébullition:; N° Mdl:; Stockage:

Column Infos

: Spiro Compounds; A spiro compound is a polycyclic compound in which two monocyclic rings share one carbon atom; the shared carbon atom is called a spiro atom. Spiro compounds have rigid structures, stable structures, and have special properties that general organic compounds do not possess, such as anomeric effect, spiro conjugation and spiro hyperconjugation. Compared with the monocyclic structure or the planar aromatic structure, the spiro structure has a larger three-dimensional structure; the heterocyclic spiro structure is also regarded as the biological isostere of some groups, which can change the drug to a certain extent. The water solubility, lipophilicity, dominant conformation and ADMET properties of the molecule make the optimized lead molecule easier to drug. Therefore, spiro compounds occupy a very important position in drug development.