Nom du produit:2-(3,4-Dihydro-2H-pyran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

IUPAC Name:2-(3,4-dihydro-2H-pyran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

CAS:1046811-99-7
Formule moléculaire:C11H19BO3
Pureté:96%
Numéro de catalogue:CM135426
Poids moléculaire:210.08

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CM135426-100mg in stock Ǥȃ
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Détails du produit

N° CAS:1046811-99-7
Formule moléculaire:C11H19BO3
Point de fusion:-
Code SMILES:CC1(C)C(C)(C)OB(C2=COCCC2)O1
Densité:
Numéro de catalogue:CM135426
Poids moléculaire:210.08
Point d'ébullition:222.3±50.0°C at 760 mmHg
N° Mdl:MFCD13195758
Stockage:

Category Infos

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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