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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, 4-bromo-5-methoxy-

COc1cccc2c1c(Br)ccn2 Request for Quotation
Chemical Name: Quinoline, 4-bromo-5-methoxy-
CAS Number: 643069-46-9
Product Number: AG00ECSL(AGN-PC-09RRF6)
Synonyms:
MDL No:
Molecular Formula: C10H8BrNO
Molecular Weight: 238.0806

Identification/Properties

Computed Properties
Molecular Weight:
238.084g/mol
XLogP3:
2.9
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:
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


4-Bromo-5-methoxyquinoline, commonly known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is frequently used in organic chemistry as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it a valuable tool for creating complex molecules with specific biological activities.In chemical synthesis, 4-Bromo-5-methoxyquinoline serves as a starting material for the construction of heterocyclic compounds, which are essential components in many drug molecules. By incorporating this compound into synthetic pathways, chemists can introduce specific functional groups and stereochemistry, enabling the creation of new compounds with improved potency, selectivity, and pharmacokinetic properties. Additionally, the bromo and methoxy substituents on the quinoline ring provide opportunities for further derivatization, allowing for the tailor-made design of molecules for various applications.Overall, the application of 4-Bromo-5-methoxyquinoline in chemical synthesis offers researchers a powerful tool for developing novel compounds with potential therapeutic or industrial significance. Its versatility and synthetic utility make it a valuable asset in the pursuit of new drug candidates and other specialized chemicals.