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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-Fluoropyridine-4-boronic acid hydrate

OB(c1ccncc1F)O.O Request for Quotation
Chemical Name: 3-Fluoropyridine-4-boronic acid hydrate
CAS Number: 1029880-18-9
Product Number: AG003JHT(AGN-PC-0WA8NX)
Synonyms:
MDL No:
Molecular Formula: C5H7BFNO3
Molecular Weight: 158.9234

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
158.923g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
159.05g/mol
Monoisotopic Mass:
159.05g/mol
Topological Polar Surface Area:
54.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
114
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (3-Fluoropyridin-4-yl)boronic acid hydrate is a versatile chemical compound widely used in organic synthesis. Its primary application lies in its role as a key building block in the preparation of various functionalized biaryls and heterocycles. This compound is particularly valuable in the field of medicinal chemistry, where it serves as a crucial intermediate for the synthesis of pharmaceuticals and agrochemicals. Additionally, (3-Fluoropyridin-4-yl)boronic acid hydrate is utilized in the development of new materials, such as liquid crystals and OLEDs, showcasing its significance across different research areas in chemical synthesis.