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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-ethoxycarbonyl-2-fluorophenyl)boronic acid

CCOC(=O)c1cccc(c1F)B(O)O Request for Quotation
Chemical Name: (3-ethoxycarbonyl-2-fluorophenyl)boronic acid
CAS Number: 1072952-52-3
Product Number: AG0084W9(AGN-PC-0786LJ)
Synonyms:
MDL No:
Molecular Formula: C9H10BFO4
Molecular Weight: 211.9827

Identification/Properties

Computed Properties
Molecular Weight:
211.983g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
212.066g/mol
Monoisotopic Mass:
212.066g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
224
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3-(Ethoxycarbonyl)-2-fluorophenyl)boronic acid is a versatile building block in chemical synthesis, particularly in the field of organic chemistry. Due to its boronic acid moiety, this compound is widely used in Suzuki-Miyaura cross-coupling reactions, where it serves as a key component for forming carbon-carbon bonds.In organic synthesis, the Suzuki-Miyaura cross-coupling reaction is a powerful tool for connecting aryl or vinyl halides with aryl or vinyl boronic acids, leading to the formation of biaryl or polyaryl compounds. This reaction is highly valuable in the pharmaceutical industry for the synthesis of complex molecules, such as drug candidates and natural products.By utilizing (3-(Ethoxycarbonyl)-2-fluorophenyl)boronic acid as a substrate in Suzuki-Miyaura cross-coupling reactions, chemists can access a wide range of functionalized aryl compounds with precision and efficiency. This compound's unique structural features make it a valuable intermediate for the synthesis of various pharmaceuticals, agrochemicals, and materials with tailored properties.