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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)-

[4-(dimethylamino)phenyl]boronic acid;hydrochloride

OB(c1ccc(cc1)N(C)C)O.Cl Request for Quotation
Chemical Name: [4-(dimethylamino)phenyl]boronic acid;hydrochloride
CAS Number: 1150114-73-0
Product Number: AG000FN6(AGN-PC-078JPF)
Synonyms:
MDL No:
Molecular Formula: C8H13BClNO2
Molecular Weight: 201.4583

Identification/Properties

Properties
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
201.457g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
201.073g/mol
Monoisotopic Mass:
201.073g/mol
Topological Polar Surface Area:
43.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
133
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(N,N-Dimethylamino)Phenylboronic Acid Hydrochloride is a versatile compound widely utilized in chemical synthesis processes. This compound serves as a valuable intermediate for the preparation of various functionalized molecules, especially in organic chemistry applications. It is commonly employed as a key building block in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds under mild reaction conditions. Additionally, this compound exhibits excellent reactivity and selectivity in the functionalization of aromatic systems, enabling the creation of complex molecular structures with high efficiency. Its hydrochloride salt form provides enhanced solubility and stability, facilitating its use in a wide range of synthetic transformations for the production of pharmaceuticals, agrochemicals, and advanced materials.