1-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-4-amine


Chemical Name: 1-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-4-amine
CAS Number: 948593-46-2
Product Number: AG01DOAQ(AGN-PC-0HZR5B)
Synonyms:
MDL No:
Molecular Formula: C11H20BN3O2
Molecular Weight: 237.1064

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound 1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-4-amine is a versatile reagent commonly used in chemical synthesis processes. It serves as a valuable building block in the creation of various organic compounds due to its unique structure and reactivity.This compound is particularly useful in metal-catalyzed cross-coupling reactions, where it acts as a boron-containing nucleophile. By participating in cross-coupling reactions with appropriate metal catalysts, 1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-4-amine can facilitate the formation of new carbon-carbon or carbon-heteroatom bonds. This reactivity makes it a key component in the synthesis of pharmaceuticals, agrochemicals, and other functional organic materials.Furthermore, the presence of both an amine and a boron moiety in this compound enables its use in a wide range of transformations, including Suzuki-Miyaura, Chan-Lam, and Buchwald-Hartwig reactions. These versatile synthetic pathways allow for the introduction of diverse functional groups, making 1-Ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-4-amine an invaluable tool in the synthesis of complex organic molecules.