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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)-

Acetamide, N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

CC(=O)Nc1ccccc1B1OC(C(O1)(C)C)(C)C Request for Quotation
Chemical Name: Acetamide, N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-
CAS Number: 380430-61-5
Product Number: AG0076GB(AGN-PC-0L0UW1)
Synonyms:
MDL No:
Molecular Formula: C14H20BNO3
Molecular Weight: 261.1245

Identification/Properties

Computed Properties
Molecular Weight:
261.128g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
261.154g/mol
Monoisotopic Mass:
261.154g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
341
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of various organic compounds. Its unique structure containing a boronic ester functionality makes it especially valuable in cross-coupling reactions, particularly in Suzuki-Miyaura coupling reactions. This compound serves as a vital component in the creation of complex molecules through the formation of carbon-carbon bonds, enabling chemists to access a diverse range of products with enhanced efficiency and precision. In addition to its utility in cross-coupling reactions, N-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide also finds applications in the synthesis of pharmaceuticals, agrochemicals, and materials science, showcasing its significance in advancing the field of organic chemistry.