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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-fluoroquinolin-3-ol

Oc1cnc2c(c1)cccc2F Request for Quotation
Chemical Name: 8-fluoroquinolin-3-ol
CAS Number: 1261784-49-9
Product Number: AG000S09(AGN-PC-0HV6NO)
Synonyms:
MDL No:
Molecular Formula: C9H6FNO
Molecular Weight: 163.1484

Identification/Properties

Computed Properties
Molecular Weight:
163.151g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
163.043g/mol
Monoisotopic Mass:
163.043g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Fluoroquinolin-3-ol, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is commonly utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and functional groups make it a valuable starting material for the synthesis of various heterocyclic compounds. In organic synthesis, 8-Fluoroquinolin-3-ol is often employed as a precursor in the development of novel drug candidates, as well as in the preparation of complex organic molecules with biological activity. Its fluorine substituent imparts specific reactivity and properties that are advantageous for creating diverse molecular structures, making it a valuable tool for synthetic chemists aiming to design and produce new compounds for various applications.