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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)-

(3,5-DIFLUOROPYRIDIN-4-YL)BORONIC ACID

OB(c1c(F)cncc1F)O Request for Quotation
Chemical Name: (3,5-DIFLUOROPYRIDIN-4-YL)BORONIC ACID
CAS Number: 956003-87-5
Product Number: AG00IJ85(AGN-PC-0KSWXP)
Synonyms:
MDL No:
Molecular Formula: C5H4BF2NO2
Molecular Weight: 158.8985664

Identification/Properties

Computed Properties
Molecular Weight:
158.899g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
159.03g/mol
Monoisotopic Mass:
159.03g/mol
Topological Polar Surface Area:
53.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
128
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:
H302-H312-H332
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(3,5-Difluoropyridin-4-yl)boronic acid, also known as $name$, is a versatile chemical compound widely used in organic synthesis. This compound is specifically valued for its boronic acid group, which is a valuable component in Suzuki-Miyaura cross-coupling reactions. In chemical synthesis, this compound serves as a key building block for the construction of complex organic molecules, allowing for the formation of new carbon-carbon bonds.$Name$ facilitates the efficient and selective formation of carbon-carbon bonds through its boronic acid functionality, enabling chemists to create a wide range of functionalized pyridine derivatives. Its application in chemical synthesis extends to the fields of pharmaceuticals, agrochemicals, and materials science, where the precise control of chemical reactions is crucial for the development of innovative compounds with diverse applications.Overall, (3,5-Difluoropyridin-4-yl)boronic acid plays a pivotal role in modern organic synthesis by enabling the strategic assembly of complex molecular structures with high efficiency and precision.