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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)-

8-Bromo-5-trifluoromethylquinoline

Brc1ccc(c2c1nccc2)C(F)(F)F Request for Quotation
Chemical Name: 8-Bromo-5-trifluoromethylquinoline
CAS Number: 917251-92-4
Product Number: AG00H1V6(AGN-PC-0WACB4)
Synonyms:
MDL No:
Molecular Formula: C10H5BrF3N
Molecular Weight: 276.0526

Identification/Properties

Computed Properties
Molecular Weight:
276.056g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
274.956g/mol
Monoisotopic Mass:
274.956g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
231
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:
Danger
UN#:
2811
Hazard Statements:
H301-H319
Precautionary Statements:
P264-P270-P280-P301+P310+P330-P305+P351+P338-P337+P313-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Bromo-5-(trifluoromethyl)quinoline is a valuable compound that finds widespread application in chemical synthesis processes. This specific molecule serves as a versatile building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties. In chemical synthesis, it acts as a key intermediate in the development of diverse organic molecules through the introduction of functional groups or the modification of existing structures. Its ability to undergo multiple reactions and participate in various transformations makes it a crucial component in the synthesis of complex organic compounds. Additionally, 8-Bromo-5-(trifluoromethyl)quinoline exhibits exceptional reactivity and selectivity, allowing chemists to efficiently access a wide range of modified quinoline derivatives with tailored properties. Its significance in chemical synthesis lies in its contribution to the development of innovative materials and therapeutic agents with enhanced functionalities and improved performance characteristics.