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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)-

(2-Formyl-3-methoxyphenyl)boronic acid

COc1cccc(c1C=O)B(O)O Request for Quotation
Chemical Name: (2-Formyl-3-methoxyphenyl)boronic acid
CAS Number: 958030-46-1
Product Number: AG00IJGF(AGN-PC-0WNGD8)
Synonyms:
MDL No: MFCD01319042
Molecular Formula: C8H9BO4
Molecular Weight: 179.9657

Identification/Properties

Computed Properties
Molecular Weight:
179.966g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
180.059g/mol
Monoisotopic Mass:
180.059g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
174
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2-Formyl-3-methoxyphenyl)boronic acid is a versatile compound widely used in chemical synthesis, notably in organic chemistry reactions. Due to its unique structure and properties, this compound is commonly employed as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its boronic acid functional group allows for easy derivatization and subsequent modification, making it a valuable tool for organic chemists. Additionally, the aldehyde and methoxy groups in its structure enable it to participate in numerous important reactions such as Suzuki-Miyaura cross-coupling reactions, allowing for efficient and selective bond formation. Overall, the (2-Formyl-3-methoxyphenyl)boronic acid plays a crucial role in the synthesis of complex organic molecules, making it indispensable in modern chemical research and development.