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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-2,4-dimethoxy-5-nitro-

COc1cc(OC)c(cc1[N+](=O)[O-])F Request for Quotation
Chemical Name: Benzene, 1-fluoro-2,4-dimethoxy-5-nitro-
CAS Number: 195136-62-0
Product Number: AG007RDM(AGN-PC-0KKMHP)
Synonyms:
MDL No:
Molecular Formula: C8H8FNO4
Molecular Weight: 201.1518

Identification/Properties

Computed Properties
Molecular Weight:
201.153g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
201.044g/mol
Monoisotopic Mass:
201.044g/mol
Topological Polar Surface Area:
64.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
208
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
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Fluoro-2,4-dimethoxy-5-nitrobenzene is a versatile compound used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries. Its fluoro, nitro, and methoxy functional groups make it a valuable intermediate in the synthesis of complex organic compounds. Its ability to undergo various reactions, such as nucleophilic substitution and reduction, makes it a key starting material for the development of new products and compounds. The presence of the fluoro group imparts specific reactivity and selectivity in chemical transformations, allowing for precise control over molecular structure and properties. Additionally, the nitro group can serve as a versatile functional group for further derivatization, expanding the scope of potential applications in chemical synthesis.