1. Home
  2. 3-Carboxyfuran-2-boronic acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-Carboxyfuran-2-boronic acid

OB(c1occc1C(=O)O)O Request for Quotation
Chemical Name: 3-Carboxyfuran-2-boronic acid
CAS Number: 1072952-23-8
Product Number: AG0084WC(AGN-PC-0WA8DQ)
Synonyms:
MDL No:
Molecular Formula: C5H5BO5
Molecular Weight: 155.9012

Identification/Properties

Computed Properties
Molecular Weight:
155.9g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
156.023g/mol
Monoisotopic Mass:
156.023g/mol
Topological Polar Surface Area:
90.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
159
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

Request for Quotation

Customer Feedback

Chemical Structure


2-Boronofuran-3-carboxylic acid is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound plays a crucial role as a boronic acid derivative in the field of organic chemistry. One of its primary applications is as a key building block in the synthesis of various pharmaceuticals and agrochemicals. Due to its functional group and boron atom, 2-Boronofuran-3-carboxylic acid can participate in diverse chemical reactions, such as Suzuki-Miyaura coupling, which is essential for forming carbon-carbon bonds. Additionally, its furan ring structure offers opportunities for creating complex molecular architectures with potential biological activity. In the realm of organic synthesis, 2-Boronofuran-3-carboxylic acid serves as a valuable tool for designing and producing novel molecules with enhanced properties and functionalities.