Nom du produit:(R)-1-Methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole

IUPAC Name:(3aR)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole

CAS:112022-83-0
Formule moléculaire:C18H20BNO
Pureté:97%
Numéro de catalogue:CM121856
Poids moléculaire:277.17

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Détails du produit

N° CAS:112022-83-0
Formule moléculaire:C18H20BNO
Point de fusion:-
Code SMILES:CB1OC(C2=CC=CC=C2)(C3=CC=CC=C3)[C@]4([H])N1CCC4
Densité:
Numéro de catalogue:CM121856
Poids moléculaire:277.17
Point d'ébullition:377.5°C at 760 mmHg
N° Mdl:MFCD00078440
Stockage:Keep in a tight container and store at ambient temperature

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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Pyrrolidines
Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.

Column Infos

Catalysts and Ligands
A catalyst refers to a substance that increases the rate of a reaction without changing the overall standard Gibbs free energy change of the reaction. Ligands represent atoms, molecules, and ions that can bond with a central atom (metal or metalloid). In general, ligands will donate at least one electron when participating in a bond. Two-phase catalysis of catalysts and ligands is the first application in the field of fluorine chemistry. The method of self-fluorine two-phase catalysis has developed rapidly, and a large number of new fluorine-based catalysts and ligands (especially phosphines) have been obtained in the field of chemistry.

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