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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-methoxycarbonyl-5-methylphenyl)boronic acid

COC(=O)c1cc(cc(c1)C)B(O)O Request for Quotation
Chemical Name: (3-methoxycarbonyl-5-methylphenyl)boronic acid
CAS Number: 929626-18-6
Product Number: AG00H32C(AGN-PC-00SB9L)
Synonyms:
MDL No:
Molecular Formula: C9H11BO4
Molecular Weight: 193.9922

Identification/Properties

Computed Properties
Molecular Weight:
193.993g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
194.075g/mol
Monoisotopic Mass:
194.075g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
207
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


(3-(Methoxycarbonyl)-5-methylphenyl)boronic acid is a versatile compound used extensively in chemical synthesis. This specific boronic acid derivative is valued for its ability to serve as a key building block in the creation of diverse organic compounds. It is particularly prized for its use in Suzuki-Miyaura cross-coupling reactions, where it acts as a crucial component in the formation of carbon-carbon bonds.In organic synthesis, this compound is employed for the functionalization of organic molecules through C-C bond formation. Its presence enables the selective introduction of the (3-(methoxycarbonyl)-5-methylphenyl) group into target molecules, allowing chemists to modify the structure of complex compounds with precision. Additionally, it can be utilized for the synthesis of various pharmaceuticals, agrochemicals, and materials due to its compatibility with a wide range of substrates.Overall, the application of (3-(Methoxycarbonyl)-5-methylphenyl)boronic acid plays a crucial role in enabling efficient and controlled chemical transformations, making it a valuable tool for synthetic chemists seeking to develop novel molecules and advance the field of organic chemistry.