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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-Benzimidazole, 4-bromo-6-(trifluoromethyl)-

Brc1cc(cc2c1[nH]cn2)C(F)(F)F Request for Quotation
Chemical Name: 1H-Benzimidazole, 4-bromo-6-(trifluoromethyl)-
CAS Number: 175135-14-5
Product Number: AG002060(AGN-PC-0KK7TG)
Synonyms:
MDL No:
Molecular Formula: C8H4BrF3N2
Molecular Weight: 265.0300

Identification/Properties

Computed Properties
Molecular Weight:
265.033g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
263.951g/mol
Monoisotopic Mass:
263.951g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
221
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-Bromo-6-(trifluoromethyl)-1H-benzo[d]imidazole is a versatile compound widely used in chemical synthesis. This compound serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. In organic synthesis, it can be employed as a key intermediate in the preparation of complex molecules by facilitating various transformations such as substitution reactions, coupling reactions, and cyclizations. Its incorporation into a molecular scaffold can enhance the stability, reactivity, and biological activity of the resulting products. Additionally, 4-Bromo-6-(trifluoromethyl)-1H-benzo[d]imidazole is commonly utilized in the development of new synthetic methodologies and the modification of existing routes to expedite the synthesis of target compounds. Its presence in the molecular structure can impart desirable physicochemical properties that are crucial for the design and optimization of novel chemical entities.