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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, 6,7-dimethoxy-

COc1cc2c(O)ccnc2cc1OC Request for Quotation
Chemical Name: 4-Quinolinol, 6,7-dimethoxy-
CAS Number: 13425-93-9
Product Number: AG0034BF(AGN-PC-0O15NE)
Synonyms:
MDL No: MFCD07368026
Molecular Formula: C11H11NO3
Molecular Weight: 205.2099

Identification/Properties

Properties
MP:
223-228°C
BP:
355.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
205.213g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
205.074g/mol
Monoisotopic Mass:
205.074g/mol
Topological Polar Surface Area:
47.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
277
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-Dimethoxyquinolin-4-ol is a versatile molecule widely utilized in chemical synthesis as a key building block. Due to its unique structure and properties, this compound serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its ability to undergo diverse chemical transformations makes it a valuable tool in the synthesis of novel compounds with potential biological activities. Specifically, 6,7-Dimethoxyquinolin-4-ol can be employed in the construction of heterocyclic frameworks, which are prevalent in many bioactive molecules. Additionally, its reactivity allows for the introduction of functional groups at specific positions, enabling the tailoring of its chemical properties for specific applications. In summary, the strategic incorporation of 6,7-Dimethoxyquinolin-4-ol in chemical synthesis enables the efficient and flexible preparation of a wide range of valuable compounds with potential for various applications.