N-methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide|1073353-58-8,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

N-methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

CON(C(=O)c1ccc(cc1)B1OC(C(O1)(C)C)(C)C)C

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Chemical Name:	N-methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
CAS Number:	1073353-58-8
Product Number:	AG003T5H(AGN-PC-07XU28)
Synonyms:
MDL No:
Molecular Formula:	C15H22BNO4
Molecular Weight:	291.1505

Identification/Properties
Safety Information
NMR Spectrum
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Identification/Properties

Properties

MP:

94-101 °C

Storage:

Keep in dry area;2-8℃;

Form:

Solid

Computed Properties

Molecular Weight:

291.154g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

291.164g/mol

Monoisotopic Mass:

291.164g/mol

Topological Polar Surface Area:

48A^2

Heavy Atom Count:

Formal Charge:

Complexity:

375

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

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 compound N-Methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide, commonly referred to as $name$, is a versatile chemical reagent utilized in modern chemical synthesis. This unique compound serves as a crucial building block in the field of organic chemistry, particularly in the formation of carbon-carbon bonds through cross-coupling reactions.$name$ is prized for its ability to participate in palladium-catalyzed coupling reactions, such as Suzuki-Miyaura cross-coupling, which are fundamental transformations in synthetic organic chemistry. By acting as a coupling partner, $name$ facilitates the construction of complex molecular structures with high efficiency and selectivity.Furthermore, $name$ is known for its stability and ease of handling, making it a valuable tool for chemists working in diverse research areas, including pharmaceuticals, materials science, and agrochemicals. Its compatibility with a wide range of functional groups and its predictable reactivity make it a preferred choice for chemists seeking to streamline their synthetic strategies and access novel molecular architectures.In summary, the application of N-Methoxy-N-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide in chemical synthesis lies in its pivotal role as a key reagent for enabling efficient carbon-carbon bond formation, thereby advancing the frontiers of modern organic chemistry.