1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine|912369-50-7,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine

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Chemical Name:	1-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]piperazine
CAS Number:	912369-50-7
Product Number:	AG006DGE(AGN-PC-01LR24)
Synonyms:
MDL No:
Molecular Formula:	C16H25BN2O2
Molecular Weight:	288.1929

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

Storage:

2-8℃;Light sensitive;Keep in dry area;

Form:

Solid

Computed Properties

Molecular Weight:

288.198g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

288.201g/mol

Monoisotopic Mass:

288.201g/mol

Topological Polar Surface Area:

33.7A^2

Heavy Atom Count:

Formal Charge:

Complexity:

345

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H302-H315-H319-H335

Precautionary Statements:

P261-P280-P301+P312-P302+P352-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

4-Piperazinylphenylboronic acid, pinacol ester is a versatile reagent that finds wide application in organic chemical synthesis. It serves as a valuable building block in the development of pharmaceuticals, agrochemicals, and materials science. With its unique properties, this compound is particularly useful in the formation of carbon-carbon and carbon-heteroatom bonds.One of the key applications of 4-Piperazinylphenylboronic acid, pinacol ester is in Suzuki-Miyaura cross-coupling reactions. This reaction allows for the rapid and efficient assembly of complex molecules by linking boronic acids with various electrophiles under mild conditions. The presence of the piperazine moiety enhances the reactivity and selectivity of this process, making it a powerful tool in the synthesis of biologically active compounds.Additionally, this compound can be employed in the construction of diverse heterocyclic structures through palladium-catalyzed coupling reactions. The resulting products can exhibit a range of pharmacological activities and can serve as valuable intermediates for further functionalization.Overall, 4-Piperazinylphenylboronic acid, pinacol ester plays a crucial role in modern organic synthesis, enabling chemists to access new molecules with potential applications in medicine, agriculture, and materials science.