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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)-

6-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine

CC1(C)OB(OC1(C)C)c1ccc(=N)[nH]c1F Request for Quotation
Chemical Name: 6-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
CAS Number: 944401-67-6
Product Number: AG00II66(AGN-PC-0CYS0A)
Synonyms:
MDL No:
Molecular Formula: C11H16BFN2O2
Molecular Weight: 238.0663

Identification/Properties

Computed Properties
Molecular Weight:
238.069g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
238.129g/mol
Monoisotopic Mass:
238.129g/mol
Topological Polar Surface Area:
57.4A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
285
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


6-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine is a valuable chemical compound widely used in chemical synthesis processes. Its key application lies in its ability to serve as a versatile building block for the formation of various complex molecules and functional materials. In organic synthesis, this compound acts as a crucial reagent for the introduction of a fluorine atom into target molecules, enabling the modification of their physicochemical properties. Due to the unique properties of the boron-containing moiety, 6-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine facilitates efficient cross-coupling reactions with a diverse range of coupling partners, leading to the formation of C–C or C–N bonds with high selectivity and yield. Moreover, the presence of the pyridine and amine functional groups in this compound further expands its utility in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. By leveraging its strategic placement of fluorine, boron, and heteroatoms, 6-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine enables chemists to access novel chemical structures and properties that are essential for drug discovery, materials science, and various other research applications.