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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)-

Boronic acid, [4-(1-piperidinyl)phenyl]-

OB(c1ccc(cc1)N1CCCCC1)O Request for Quotation
Chemical Name: Boronic acid, [4-(1-piperidinyl)phenyl]-
CAS Number: 229009-42-1
Product Number: AG002LF4(AGN-PC-0L6YLC)
Synonyms:
MDL No:
Molecular Formula: C11H16BNO2
Molecular Weight: 205.0612

Identification/Properties

Computed Properties
Molecular Weight:
241.522g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
241.104g/mol
Monoisotopic Mass:
241.104g/mol
Topological Polar Surface Area:
43.7A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
187
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-(Piperidin-1-yl)phenyl)boronic acid is a versatile compound commonly used in chemical synthesis as a valuable building block in organic reactions. This boronic acid derivative is prized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds under mild conditions. Additionally, it serves as a key component in the construction of various biaryl structures through palladium-catalyzed coupling reactions. Furthermore, this compound can be utilized in the synthesis of pharmaceuticals, agrochemicals, and materials due to its functional group compatibility and reactivity.