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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)-

3-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid, pinacol ester

CON(C(=O)c1cccc(c1)B1OC(C(O1)(C)C)(C)C)C Request for Quotation
Chemical Name: 3-(N,O-Dimethylhydroxylaminocarbonyl)phenylboronic acid, pinacol ester
CAS Number: 957061-17-5
Product Number: AG003I9L(AGN-PC-0WA7MI)
Synonyms:
MDL No:
Molecular Formula: C15H22BNO4
Molecular Weight: 291.1505

Identification/Properties

Properties
MP:
69-72℃
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
291.154g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
291.164g/mol
Monoisotopic Mass:
291.164g/mol
Topological Polar Surface Area:
48A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
383
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


N-Methoxy-N-methyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide serves as a versatile building block in modern chemical synthesis. This compound plays a crucial role in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. Through this process, N-Methoxy-N-methyl-3-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide can be effectively incorporated into more complex molecular structures, making it an invaluable tool for organic chemists seeking to create novel compounds with specific functionalities and properties. Additionally, its unique structure containing both boron and amide functional groups imparts distinctive reactivity, offering opportunities for the development of innovative synthetic strategies and the construction of diverse molecular architectures.