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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-chloro-

Clc1ccc2c(c1)c(O)ccn2 Request for Quotation
Chemical Name: 4-Quinolinol, 6-chloro-
CAS Number: 23432-43-1
Product Number: AG002N85(AGN-PC-0O83NP)
Synonyms:
MDL No:
Molecular Formula: C9H6ClNO
Molecular Weight: 179.6030

Identification/Properties

Computed Properties
Molecular Weight:
179.603g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
179.014g/mol
Monoisotopic Mass:
179.014g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
227
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Chloroquinolin-4-ol, known for its aromatic structure and chlorine substitution, serves as a valuable reagent in chemical synthesis. Its unique properties make it a versatile building block in the creation of various organic compounds. In the field of medicinal chemistry, 6-Chloroquinolin-4-ol is often utilized as a key intermediate for the synthesis of pharmaceuticals and biologically active molecules. Its reactivity allows for the introduction of functional groups at specific positions, enabling the fine-tuning of molecular structures for desired biological activities. Additionally, this compound can participate in various transformations such as halogenation, alkylation, and cross-coupling reactions, facilitating the synthesis of complex organic molecules. Researchers and chemists extensively employ 6-Chloroquinolin-4-ol as a strategic tool in the development of new drug candidates and chemical probes for biological studies.