Nom du produit:2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)-1,2,3,4-tetrahydroisoquinoline

IUPAC Name:2-{[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}-1,2,3,4-tetrahydroisoquinoline

CAS:1315281-49-2
Formule moléculaire:C22H28BNO2
Pureté:95%
Numéro de catalogue:CM207429
Poids moléculaire:349.28

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Détails du produit

N° CAS:1315281-49-2
Formule moléculaire:C22H28BNO2
Point de fusion:-
Code SMILES:CC1(C)C(C)(C)OB(C2=CC=C(C=C2)CN3CC4=C(C=CC=C4)CC3)O1
Densité:
Numéro de catalogue:CM207429
Poids moléculaire:349.28
Point d'ébullition:
N° Mdl:MFCD16294539
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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Tetrahydroisoquinolines
Tetrahydroisoquinoline is an organic compound with the chemical formula C9H11N. It is classified as a secondary amine, obtained from isoquinoline by hydrogenation. The tetrahydroisoquinoline moiety forms the backbone of several natural, synthetic and semi-synthetic drugs approved for the treatment of cancer, pain, gout and various neurodegenerative diseases.

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