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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-methyl-1-propenyl)-

OB(C=C(C)C)O Request for Quotation
Chemical Name: Boronic acid, (2-methyl-1-propenyl)-
CAS Number: 14559-88-7
Product Number: AG001D7K(AGN-PC-0KKPFG)
Synonyms:
MDL No:
Molecular Formula: C4H9BO2
Molecular Weight: 99.9241

Identification/Properties

Computed Properties
Molecular Weight:
99.924g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
100.07g/mol
Monoisotopic Mass:
100.07g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
73.8
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


(2,2-Dimethylethenyl)boronic acid is a versatile compound that finds widespread application in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in organic chemistry.In chemical synthesis, (2,2-Dimethylethenyl)boronic acid functions as a key reagent in Suzuki-Miyaura cross-coupling reactions. This important reaction allows for the formation of carbon-carbon bonds under mild conditions, enabling chemists to efficiently assemble complex organic molecules. By serving as a coupling partner, (2,2-Dimethylethenyl)boronic acid facilitates the introduction of diverse functional groups and substituents into the target molecule.Moreover, (2,2-Dimethylethenyl)boronic acid can also participate in various other transformations, such as C-H activation, carbonylation, and halogenation reactions. Its versatile nature and compatibility with a wide range of functional groups make it a valuable reagent for constructing pharmaceuticals, agrochemicals, and materials with tailored properties.Overall, the application of (2,2-Dimethylethenyl)boronic acid in chemical synthesis highlights its significance as a powerful tool for building complex molecular structures and advancing the field of organic chemistry.