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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)-

Quinoline, 6-methoxy-2-methyl-

COc1ccc2c(c1)ccc(n2)C Request for Quotation
Chemical Name: Quinoline, 6-methoxy-2-methyl-
CAS Number: 1078-28-0
Product Number: AG008RJ0(AGN-PC-0JL9U6)
Synonyms:
MDL No:
Molecular Formula: C11H11NO
Molecular Weight: 173.2111

Identification/Properties

Computed Properties
Molecular Weight:
173.215g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
173.084g/mol
Monoisotopic Mass:
173.084g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
172
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Methoxy-2-methylquinoline is an important compound used in chemical synthesis as a versatile building block. In the field of organic chemistry, this molecule serves as a key precursor in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable intermediate in the production of complex organic compounds. In particular, 6-Methoxy-2-methylquinoline is often employed in the creation of heterocyclic compounds for drug discovery and development. Its presence in the synthesis pathway enhances the molecular diversity and biological activity of the final products. Additionally, this compound exhibits interesting properties that have found applications in the fields of materials science and catalysis. Its role in chemical synthesis highlights its significance as a versatile building block with a wide range of applications in the realm of organic chemistry.