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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, 1-(4-piperidinyl)-2-(trifluoromethyl)-

FC(c1nc2c(n1C1CCNCC1)cccc2)(F)F Request for Quotation
Chemical Name: 1H-Benzimidazole, 1-(4-piperidinyl)-2-(trifluoromethyl)-
CAS Number: 742076-06-8
Product Number: AG005YZL(AGN-PC-07HB1F)
Synonyms:
MDL No:
Molecular Formula: C13H14F3N3
Molecular Weight: 269.2656

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
269.271g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
269.114g/mol
Monoisotopic Mass:
269.114g/mol
Topological Polar Surface Area:
29.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
315
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


The chemical compound 1-(Piperidin-4-yl)-2-(trifluoromethyl)-1H-benzo[d]imidazole serves as a valuable tool in chemical synthesis processes. This versatile compound is utilized as a key building block in the creation of various organic molecules and pharmaceuticals. Its unique structure, featuring a piperidine ring and a trifluoromethyl group attached to a benzimidazole core, imparts distinct reactivity and functionality essential for the formation of complex molecular structures. In synthesis, this compound can be employed to introduce specific functional groups, modify molecular properties, and enhance the bioactivity of final products. Its strategic placement can enable the creation of diverse chemical architectures with precision and efficiency. By incorporating 1-(Piperidin-4-yl)-2-(trifluoromethyl)-1H-benzo[d]imidazole into synthetic routes, chemists can achieve tailored and sophisticated chemical transformations, making it a valuable asset in the realm of chemical synthesis.