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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-methoxy-3-nitro-5-(trifluoromethyl)-

COc1cc(cc(c1)C(F)(F)F)[N+](=O)[O-] Request for Quotation
Chemical Name: Benzene, 1-methoxy-3-nitro-5-(trifluoromethyl)-
CAS Number: 328-79-0
Product Number: AG00BXE0(AGN-PC-0JS9KH)
Synonyms:
MDL No:
Molecular Formula: C8H6F3NO3
Molecular Weight: 221.1333

Identification/Properties

Computed Properties
Molecular Weight:
221.135g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
221.03g/mol
Monoisotopic Mass:
221.03g/mol
Topological Polar Surface Area:
55A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
238
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


3-Methoxy-5-nitrobenzotrifluoride, also known as MNBF, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable building block in the creation of various organic compounds. MNBF is commonly employed in the pharmaceutical industry for the synthesis of potential drug candidates and active pharmaceutical ingredients.In organic synthesis, MNBF serves as a key intermediate in the preparation of complex molecules with specific functionalities. Its nitro and methoxy groups provide opportunities for further functionalization through various chemical reactions, such as reduction, substitution, and coupling reactions. MNBF's trifluoromethyl group enhances the compound's stability and lipophilicity, making it suitable for applications in medicinal chemistry.Additionally, MNBF can be utilized in the development of agrochemicals, materials science, and other specialty chemicals. Its compatibility with a wide range of reaction conditions and compatibility with various functional groups make it a valuable tool for synthetic chemists seeking to create novel compounds with tailored properties.Overall, 3-Methoxy-5-nitrobenzotrifluoride plays a crucial role in modern chemical synthesis, offering unique opportunities for the construction of diverse molecular architectures with potential applications in pharmaceuticals, agrochemicals, and materials science.