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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, [2-[(phenylamino)methyl]phenyl]-

OB(c1ccccc1CNc1ccccc1)O Request for Quotation
Chemical Name: Boronic acid, [2-[(phenylamino)methyl]phenyl]-
CAS Number: 327096-48-0
Product Number: AG00CLSV(AGN-PC-0NHUJB)
Synonyms:
MDL No:
Molecular Formula: C13H14BNO2
Molecular Weight: 227.0668

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
227.07g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
227.112g/mol
Monoisotopic Mass:
227.112g/mol
Topological Polar Surface Area:
52.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
220
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2-((Phenylamino)methyl)phenyl)boronic acid is a versatile reagent widely used in chemical synthesis for its unique properties. This compound serves as a key building block in the creation of various organic molecules due to its ability to participate in diverse reactions. In particular, it is commonly employed in Suzuki-Miyaura cross-coupling reactions, where it acts as a boron source to form carbon-carbon bonds.Additionally, (2-((Phenylamino)methyl)phenyl)boronic acid is valuable in the synthesis of pharmaceuticals, agrochemicals, and materials science. Its compatibility with a range of functional groups makes it highly desirable for constructing complex molecular structures with precision and efficiency. The compound's role in facilitating the formation of aryl-aryl bonds makes it a crucial component in the development of new drugs and other bioactive compounds.In summary, (2-((Phenylamino)methyl)phenyl)boronic acid is an indispensable tool in organic synthesis, enabling chemists to access a wide array of molecules with diverse applications and properties.