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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)-

2-Bromo-3-(Difluoromethoxy)-Pyridine

FC(Oc1cccnc1Br)F Request for Quotation
Chemical Name: 2-Bromo-3-(Difluoromethoxy)-Pyridine
CAS Number: 947249-27-6
Product Number: AG00IIHD(AGN-PC-0WAG7A)
Synonyms:
MDL No:
Molecular Formula: C6H4BrF2NO
Molecular Weight: 224.0029

Identification/Properties

Computed Properties
Molecular Weight:
224.005g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
222.944g/mol
Monoisotopic Mass:
222.944g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
125
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-3-(difluoromethoxy)pyridine, also known as $name$, is a specialized compound widely used in chemical synthesis for its unique properties and versatile applications. As a halogenated pyridine derivative, $name$ serves as an important building block in the development of novel pharmaceuticals, agrochemicals, and organic materials.Due to its strategic combination of bromine and difluoromethoxy functional groups, 2-Bromo-3-(difluoromethoxy)pyridine exhibits enhanced reactivity and compatibility with a variety of chemical reactions. One of the key applications of this compound lies in its use as a halogenated intermediate for the synthesis of complex organic molecules. The presence of bromine and difluoromethoxy moieties in $name$ enables chemists to introduce these specific substituents into target molecules with precision, facilitating the creation of molecules with desired biological activities or physical properties.Moreover, 2-Bromo-3-(difluoromethoxy)pyridine plays a crucial role in cross-coupling reactions, where it can participate as a coupling partner to form new carbon-carbon or carbon-heteroatom bonds. This reactivity makes $name$ a valuable tool in the construction of functionalized aromatic compounds and heterocycles, which are fundamental structural motifs in many biologically active molecules and advanced materials.In summary, the application of 2-Bromo-3-(difluoromethoxy)pyridine in chemical synthesis offers chemists a powerful tool for the design and synthesis of diverse functional molecules with potential applications in pharmaceutical, agricultural, and materials science research.