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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)-

Benzene, 1-fluoro-3-methoxy-2-nitro-

COc1cccc(c1[N+](=O)[O-])F Request for Quotation
Chemical Name: Benzene, 1-fluoro-3-methoxy-2-nitro-
CAS Number: 641-49-6
Product Number: AG0032RI(AGN-PC-0KL1W5)
Synonyms:
MDL No:
Molecular Formula: C7H6FNO3
Molecular Weight: 171.1258

Identification/Properties

Properties
MP:
43°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
171.127g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
171.033g/mol
Monoisotopic Mass:
171.033g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
171
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:
Danger
UN#:
2811
Hazard Statements:
H301-H315-H319-H335-H350
Precautionary Statements:
P201-P261-P301+P310-P305+P351+P338-P308+P313
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Fluoro-2-nitroanisole is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to undergo a range of functional group transformations.One of the main applications of 3-Fluoro-2-nitroanisole is its involvement in the synthesis of heterocyclic compounds. By undergoing various functionalization reactions, such as reduction, substitution, or coupling reactions, this compound can be incorporated into complex molecular structures, enabling the creation of bioactive molecules and intermediates used in drug discovery.Furthermore, 3-Fluoro-2-nitroanisole is commonly employed in the preparation of materials for organic electronic devices. Its unique electronic properties and ability to act as a precursor for π-conjugated systems make it a valuable component in the development of organic semiconductors and light-emitting materials.Additionally, this compound can be used in the production of specialty chemicals and advanced materials, where its specific fluorine and nitro functionalities play a crucial role in imparting desired properties to the final products. Overall, 3-Fluoro-2-nitroanisole is an important intermediate in chemical synthesis, offering a wide range of applications in diverse industries.