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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,B-[5-[(cyclohexylamino)carbonyl]-2-fluorophenyl]-

O=C(c1ccc(c(c1)B(O)O)F)NC1CCCCC1 Request for Quotation
Chemical Name: Boronic acid,B-[5-[(cyclohexylamino)carbonyl]-2-fluorophenyl]-
CAS Number: 874289-44-8
Product Number: AG00GSYH(AGN-PC-0VDJD8)
Synonyms:
MDL No:
Molecular Formula: C13H17BFNO3
Molecular Weight: 265.0884

Identification/Properties

Computed Properties
Molecular Weight:
265.091g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
265.129g/mol
Monoisotopic Mass:
265.129g/mol
Topological Polar Surface Area:
69.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
310
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-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


B-[5-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]boronic acid is a versatile compound commonly used in chemical synthesis as a key building block. This unique molecule plays a crucial role in various synthetic processes, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.In organic chemistry, B-[5-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]boronic acid is frequently employed as a boronic acid derivative for Suzuki-Miyaura cross-coupling reactions. This powerful reaction enables the formation of complex organic structures by coupling aryl or vinyl boronic acids with organic halides or pseudohalides in the presence of a palladium catalyst. The resulting products are essential in the synthesis of pharmaceuticals, agrochemicals, and materials science.Furthermore, this compound serves as a valuable reagent in the preparation of functionalized materials, such as polymers, dendrimers, and ligands for catalysis. Its unique structure featuring a boronic acid moiety and a fluorophenyl group imparts specific reactivity and selectivity in various transformations, making it a sought-after component in modern organic chemistry research.Overall, B-[5-[(Cyclohexylamino)carbonyl]-2-fluorophenyl]boronic acid's broad application spectrum in chemical synthesis highlights its significance as a versatile and indispensable tool for constructing complex molecules with precision and efficiency.