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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)-

Pyridine, 3-(3-fluoro-5-nitrophenoxy)-

Fc1cc(Oc2cccnc2)cc(c1)[N+](=O)[O-] Request for Quotation
Chemical Name: Pyridine, 3-(3-fluoro-5-nitrophenoxy)-
CAS Number: 803700-29-0
Product Number: AG008MSS(AGN-PC-0BSBIG)
Synonyms:
MDL No:
Molecular Formula: C11H7FN2O3
Molecular Weight: 234.1833

Identification/Properties

Computed Properties
Molecular Weight:
234.186g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
234.044g/mol
Monoisotopic Mass:
234.044g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
272
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(3-Fluoro-5-nitrophenoxy)pyridine, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique chemical structure makes it a valuable building block for the creation of various organic compounds with specific properties and functions. In organic synthesis, $name$ plays a crucial role as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and advanced materials. Its reactivity and compatibility with a wide range of functional groups make it a preferred choice for constructing complex molecular structures in the laboratory. Additionally, the presence of the fluoro and nitro groups in $name$ offers opportunities for further functionalization and modification through various chemical reactions, enabling the synthesis of tailored molecules for targeted applications. This compound's significance in chemical synthesis lies in its ability to facilitate the development of novel compounds with diverse applications in the fields of medicine, agriculture, and materials science.