Nom du produit:1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-yl-5-boronic acid

IUPAC Name:[1-(oxan-2-yl)-1H-indazol-5-yl]boronic acid

CAS:1562245-02-6
Formule moléculaire:C12H15BN2O3
Pureté:95%
Numéro de catalogue:CM111399
Poids moléculaire:246.07

Unité d'emballage Stock disponible Prix($) Quantité
CM111399-250mg in stock ȐǶ
CM111399-1g in stock ƃŵƛ
CM111399-5g in stock ȡǑȐ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:1562245-02-6
Formule moléculaire:C12H15BN2O3
Point de fusion:-
Code SMILES:OB(C1=CC2=C(N(C3CCCCO3)N=C2)C=C1)O
Densité:
Numéro de catalogue:CM111399
Poids moléculaire:246.07
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Indazoles
Indazoles are a class of organic heterocyclic compounds, also known as 1,2-diazaindene and benzopyrazole. Indazole is a good bioisomer of phenol, which is more lipophilic than phenol and less prone to phase I and II metabolism. Indazole derivatives have a wide range of biological activities, and it has been confirmed that indazole compounds have anti-tumor, analgesic, anti-inflammatory and other drug activities. Anticancer is the most important application field of indazole drugs. Renal cell carcinoma, solid tumor, nausea and vomiting caused by chemotherapy and leukemia are the main indications of this structural backbone drug.
Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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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.

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