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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-methyl-6-nitro-

Fc1cc(C)c(c(c1)[N+](=O)[O-])N Request for Quotation
Chemical Name: Benzenamine, 4-fluoro-2-methyl-6-nitro-
CAS Number: 147285-87-8
Product Number: AG001ERU(AGN-PC-0N3ESC)
Synonyms:
MDL No:
Molecular Formula: C7H7FN2O2
Molecular Weight: 170.1411

Identification/Properties

Properties
MP:
98-100°
BP:
312.1°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
170.143g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
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:
183
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Benzenamine, 4-fluoro-2-methyl-6-nitro-, is a versatile compound widely used in chemical synthesis. With its unique chemical structure, this compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its presence of a nitro group enhances its reactivity, making it a significant intermediate in the production of fine chemicals. This compound is particularly utilized in the synthesis of dyes, pharmaceuticals, and specialty chemicals due to its ability to introduce specific functional groups during reactions. Its role in organic synthesis facilitates the preparation of complex molecules with enhanced properties, enabling researchers and chemists to explore new avenues in drug development and material science.