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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-methoxy-6,8-dimethylquinoline

COc1ccc2c(n1)c(C)cc(c2)C Request for Quotation
Chemical Name: 2-methoxy-6,8-dimethylquinoline
CAS Number: 861581-28-4
Product Number: AG003HJK(AGN-PC-09PZQE)
Synonyms:
MDL No:
Molecular Formula: C12H13NO
Molecular Weight: 187.2377

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
187.242g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
187.1g/mol
Monoisotopic Mass:
187.1g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
195
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


2-Methoxy-6,8-dimethylquinoline, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a building block in various organic reactions and transformations. Its unique structure and reactivity make it valuable in the synthesis of complex molecules, pharmaceuticals, and agrochemicals.One of the key applications of 2-Methoxy-6,8-dimethylquinoline in chemical synthesis is its use as a ligand in transition metal-catalyzed reactions. The quinoline moiety in this compound can coordinate with transition metals such as palladium and ruthenium, enabling the formation of stable complexes that can catalyze a range of important reactions. These metal-ligand complexes are particularly effective in promoting processes such as cross-coupling reactions, C-H functionalization, and cycloadditions.Additionally, 2-Methoxy-6,8-dimethylquinoline can also act as a nucleophilic or electrophilic component in various synthetic transformations. Its methoxy and methyl substituents provide steric and electronic effects that influence its reactivity and selectivity in different reactions. This compound can participate in processes like nucleophilic substitution, Friedel-Crafts reactions, and oxidative transformations, offering a diverse toolkit for synthetic chemists to access a wide range of chemical structures.Overall, the versatility and reactivity of 2-Methoxy-6,8-dimethylquinoline make it a valuable tool in chemical synthesis, enabling the construction of complex molecules and facilitating the development of new materials and compounds.