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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)-

1H-Imidazole, 4-methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-

Cc1ncn(c1)c1cc(cc(c1)C(F)(F)F)[N+](=O)[O-] Request for Quotation
Chemical Name: 1H-Imidazole, 4-methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-
CAS Number: 916975-92-3
Product Number: AG00391U(AGN-PC-01LQA4)
Synonyms:
MDL No:
Molecular Formula: C11H8F3N3O2
Molecular Weight: 271.1953

Identification/Properties

Computed Properties
Molecular Weight:
271.199g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
271.057g/mol
Monoisotopic Mass:
271.057g/mol
Topological Polar Surface Area:
63.6A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
345
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-Methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-1H-imidazole is a versatile compound that finds extensive application in chemical synthesis processes. Its unique chemical structure allows for its incorporation into various reactions to produce valuable intermediates and final products in the field of organic chemistry.In chemical synthesis, 4-Methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-1H-imidazole serves as a key building block for the creation of complex molecules. It can participate in different types of reactions such as nucleophilic substitution, condensation, and cyclization reactions. The presence of the nitro and trifluoromethyl groups in the molecule imparts specific reactivity and functionality, enabling the formation of diverse chemical connections with other compounds.One of the significant applications of 4-Methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-1H-imidazole in chemical synthesis is its role as a precursor in the synthesis of pharmaceutical compounds. By selectively modifying its functional groups or utilizing its core structure as a scaffold, chemists can generate new drug candidates with potential therapeutic benefits. Additionally, this compound can be employed in the production of agrochemicals, dyes, and materials with specialized properties.Overall, the use of 4-Methyl-1-[3-nitro-5-(trifluoromethyl)phenyl]-1H-imidazole in chemical synthesis offers a strategic approach to designing and constructing intricate organic molecules for a wide range of applications in industries such as pharmaceuticals, agrochemicals, and materials science.