Produktname: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
Molekulare Formel:C22H28BNO2
Reinheit:95%
Katalognummer:CM207429
Molekulargewicht:349.28

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Produkt-Details

CAS-Nr.:1315281-49-2
Molekulare Formel:C22H28BNO2
Schmelzpunkt:-
SMILES-Code:CC1(C)C(C)(C)OB(C2=CC=C(C=C2)CN3CC4=C(C=CC=C4)CC3)O1
Dichte:
Katalognummer:CM207429
Molekulargewicht:349.28
Siedepunkt:
Mdl-Nr.:MFCD16294539
Lagerung:

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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