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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-fluoro-4,5-dimethoxyaniline

COc1cc(F)c(cc1OC)N Request for Quotation
Chemical Name: 2-fluoro-4,5-dimethoxyaniline
CAS Number: 397-75-1
Product Number: AG01AGHK(AG01AGHK)
Synonyms:
MDL No:
Molecular Formula: C8H10FNO2
Molecular Weight: 171.1689

Identification/Properties

Computed Properties
Molecular Weight:
171.171g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
171.07g/mol
Monoisotopic Mass:
171.07g/mol
Topological Polar Surface Area:
44.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
145
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-4,5-dimethoxyaniline is a highly versatile compound that finds extensive application in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block in organic chemistry.In chemical synthesis, 2-Fluoro-4,5-dimethoxyaniline is commonly utilized as a precursor in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its fluorinated moiety imparts distinct properties to the final products, making it particularly valuable in medicinal chemistry and materials science.Furthermore, the presence of both a fluoro and dimethoxy groups in its structure enables diverse functionalization reactions, allowing for the creation of a wide range of derivative compounds with tailored properties. This flexibility makes 2-Fluoro-4,5-dimethoxyaniline a key intermediate in the synthesis of complex molecules and advanced materials.Overall, the strategic incorporation of 2-Fluoro-4,5-dimethoxyaniline in chemical transformations offers synthetic chemists a powerful tool for designing and synthesizing novel compounds with enhanced biological, physical, or chemical properties.