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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol

O=C(N1CCN(CC1)Cc1ccccc1B1OC(C(O1)(C)C)(C)C)OC(C)(C)C Request for Quotation
Chemical Name: 2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol
CAS Number: 1012785-48-6
Product Number: AG000447(AGN-PC-0WA53J)
Synonyms:
MDL No:
Molecular Formula: C22H35BN2O4
Molecular Weight: 402.3353

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol is a versatile reagent commonly used in chemical synthesis for the formation of carbon-carbon bonds. This compound serves as a powerful tool in organic chemistry, particularly in the field of medicinal chemistry and drug discovery. It is utilized for its ability to form stable boronate esters with various electrophiles, enabling the selective functionalization of molecules.One key application of 2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol is in Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl or vinyl boronic acid with an organic halide or pseudohalide to form a new carbon-carbon bond. By utilizing this boronic acid derivative, chemists can efficiently synthesize complex organic molecules with high selectivity and yield.Additionally, this compound can be employed in the synthesis of pharmaceutical intermediates, agrochemicals, and materials chemistry. Its unique structure, combining the boronic acid moiety with a piperazine group, offers opportunities for the design and development of novel molecules with diverse biological activities.Overall, 2-(4-Boc-piperazin-1yl)methylphenylboronic acid, pinacol plays a crucial role in modern organic synthesis by enabling the construction of complex molecules through efficient and controlled cross-coupling reactions.