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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)-

(4-FLUORO-3-NITROPHENYL) METHANAMINE

NCc1ccc(c(c1)[N+](=O)[O-])F Request for Quotation
Chemical Name: (4-FLUORO-3-NITROPHENYL) METHANAMINE
CAS Number: 771581-73-8
Product Number: AG005PCP(AGN-PC-01WC35)
Synonyms:
MDL No:
Molecular Formula: C7H7FN2O2
Molecular Weight: 170.1411

Identification/Properties

Computed Properties
Molecular Weight:
170.143g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
170.049g/mol
Monoisotopic Mass:
170.049g/mol
Topological Polar Surface Area:
71.8A^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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (4-Fluoro-3-nitrophenyl)methanamine, also known as $name$, is a versatile compound widely used in chemical synthesis. It serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. When employed in chemical reactions, $name$ plays a crucial role in introducing functional groups and modifying the structure of organic molecules. Its unique properties make it an essential reagent for the synthesis of intricate compounds with specific applications in the field of medicinal chemistry and material science. By utilizing (4-Fluoro-3-nitrophenyl)methanamine, chemists can streamline the synthesis process, leading to the efficient production of desired organic compounds with enhanced properties.