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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)-

Benzenamine, 4-fluoro-2-iodo-5-methyl-

Fc1cc(I)c(cc1C)N Request for Quotation
Chemical Name: Benzenamine, 4-fluoro-2-iodo-5-methyl-
CAS Number: 85233-15-4
Product Number: AG008FUE(AGN-PC-04Z0YV)
Synonyms:
MDL No:
Molecular Formula: C7H7FIN
Molecular Weight: 251.0401

Identification/Properties

Computed Properties
Molecular Weight:
251.043g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
250.961g/mol
Monoisotopic Mass:
250.961g/mol
Topological Polar Surface Area:
26A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Fluoro-2-iodo-5-methylaniline, commonly abbreviated as $name$, is a versatile compound that finds wide applications in chemical synthesis. This compound is particularly valued for its role as a building block in the synthesis of various organic molecules due to its unique structural properties.One key application of 4-Fluoro-2-iodo-5-methylaniline in chemical synthesis is its use as a precursor in the preparation of pharmaceutical intermediates. By serving as a starting material in the synthesis of complex molecules, this compound plays a crucial role in the development of new drugs and therapeutic agents. The strategic placement of the fluoro and iodo substituents on the aromatic ring enables specific functional group transformations, making it a valuable tool for medicinal chemists.Additionally, 4-Fluoro-2-iodo-5-methylaniline is employed in the production of agrochemicals and specialty chemicals. Its ability to undergo various chemical reactions, such as Suzuki coupling and halogenation, allows for the efficient synthesis of agricultural compounds and fine chemicals with tailored properties. This compound serves as a key intermediate in the construction of pesticide molecules and other agrochemicals essential for modern agriculture.Moreover, the presence of a fluorine atom in conjunction with an iodo group in 4-Fluoro-2-iodo-5-methylaniline imparts unique reactivity and selectivity in cross-coupling reactions. This enables the selective formation of carbon-carbon and carbon-heteroatom bonds, making it a valuable tool in designing and synthesizing advanced materials, dyes, and polymers with specific characteristics and functionalities.In summary, 4-Fluoro-2-iodo-5-methylaniline plays a vital role in chemical synthesis as a versatile building block for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its distinctive structural features and reactivity make it an indispensable tool for synthetic chemists in the development of new and innovative compounds for various applications.