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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)-

2(1H)-Quinolinone, 4-(trifluoromethyl)-

O=c1[nH]c2ccccc2c(c1)C(F)(F)F Request for Quotation
Chemical Name: 2(1H)-Quinolinone, 4-(trifluoromethyl)-
CAS Number: 25199-84-2
Product Number: AG002QV4(AGN-PC-0KKN5I)
Synonyms:
MDL No:
Molecular Formula: C10H6F3NO
Molecular Weight: 213.1559

Identification/Properties

Properties
MP:
>240 °C
BP:
284.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
213.159g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
0
Exact Mass:
213.04g/mol
Monoisotopic Mass:
213.04g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
308
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:
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


2-Hydroxy-4-(trifluoromethyl)quinoline, also known as HFQM, is a versatile compound widely used in chemical synthesis. This specialized compound plays a crucial role in various organic reactions and processes, offering unique properties that enable its application in a range of synthesis pathways. With its distinct structure and functional groups, 2-Hydroxy-4-(trifluoromethyl)quinoline serves as a valuable building block in the creation of novel molecules and pharmaceuticals. In chemical synthesis, this compound functions as a key intermediate, facilitating the production of specialized materials and compounds through precise manipulation of its reactive sites. Its incorporation in organic reactions leads to the formation of new compounds with diverse properties, making it an essential component in the realm of synthetic chemistry. Whether employed in pharmaceutical development, material science, or other research fields, 2-Hydroxy-4-(trifluoromethyl)quinoline stands out as a powerful tool for advancing innovation and discovery in the realm of chemical synthesis.