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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-(4-morpholinylmethyl)phenyl]-

OB(c1ccc(cc1)CN1CCOCC1)O Request for Quotation
Chemical Name: Boronic acid, [4-(4-morpholinylmethyl)phenyl]-
CAS Number: 279262-23-6
Product Number: AG00BCUV(AGN-PC-0NE6MU)
Synonyms:
MDL No:
Molecular Formula: C11H16BNO3
Molecular Weight: 221.0606

Identification/Properties

Properties
MP:
85℃
BP:
382.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
221.063g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
221.122g/mol
Monoisotopic Mass:
221.122g/mol
Topological Polar Surface Area:
52.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
201
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Morpholinomethyl)phenylboronic acid is a versatile compound widely used in chemical synthesis as a key building block in the formation of various organic molecules. This particular boronic acid derivative is especially valued for its ability to undergo Suzuki-Miyaura cross-coupling reactions, a crucial tool in modern organic chemistry for creating complex structures efficiently. The presence of the morpholinomethyl group provides enhanced stability and reactivity, making it a valuable component in the construction of pharmaceuticals, agrochemicals, and advanced materials. Additionally, this compound can participate in a range of transformations, such as C-H activation and carbon-carbon bond formations, further expanding its utility in synthetic chemistry.