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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, 7-bromo-2-methoxy-

COc1ccc2c(n1)cc(cc2)Br Request for Quotation
Chemical Name: Quinoline, 7-bromo-2-methoxy-
CAS Number: 99455-08-0
Product Number: AG00IKAG(AGN-PC-000R15)
Synonyms:
MDL No:
Molecular Formula: C10H8BrNO
Molecular Weight: 238.0806

Identification/Properties

Computed Properties
Molecular Weight:
238.084g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
236.979g/mol
Monoisotopic Mass:
236.979g/mol
Topological Polar Surface Area:
22.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
176
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-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


7-Bromo-2-methoxyquinoline is a highly versatile compound widely utilized in chemical synthesis for its ability to serve as a valuable building block in the creation of various organic molecules. With its unique structure and reactive bromine functionality, this compound plays a crucial role in the preparation of complex organic compounds through a range of synthetic pathways. Specifically, 7-Bromo-2-methoxyquinoline is frequently employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials due to its capability to undergo diverse chemical transformations, including substitution, addition, and coupling reactions. Furthermore, its methoxy group offers additional opportunities for chemical modification, enabling the tailoring of molecular properties for specific applications. In chemical synthesis, 7-Bromo-2-methoxyquinoline acts as a key intermediate, enabling the construction of more intricate molecular structures with enhanced functionalities and potential applications in various industries.