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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)-

4-Quinolinol,6,8-dichloro-2-(trifluoromethyl)-

Clc1cc(Cl)c2c(c1)c(O)cc(n2)C(F)(F)F Request for Quotation
Chemical Name: 4-Quinolinol,6,8-dichloro-2-(trifluoromethyl)-
CAS Number: 18706-23-5
Product Number: AG003N1H(AGN-PC-0QG54U)
Synonyms:
MDL No:
Molecular Formula: C10H4Cl2F3NO
Molecular Weight: 282.0461

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
282.043g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
0
Exact Mass:
280.962g/mol
Monoisotopic Mass:
280.962g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
369
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


6,8-Dichloro-2-(trifluoromethyl)quinolin-4-ol serves as a versatile building block in chemical synthesis. This compound plays a key role in the production of pharmaceuticals, agrochemicals, and materials due to its unique structural properties. Its presence of chloro and trifluoromethyl groups enables it to participate in a variety of reactions, including nucleophilic substitutions and cross-coupling processes. In pharmaceutical synthesis, this compound can be utilized for the construction of heterocyclic frameworks, making it a valuable tool in drug discovery research. Additionally, in agrochemical synthesis, 6,8-Dichloro-2-(trifluoromethyl)quinolin-4-ol can be employed to develop novel pesticides and herbicides with enhanced biological activities. Its application extends to material science, where it can be incorporated into functional materials for various industrial applications.