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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)-

3-Quinolinol, 4-bromo-2-methyl-

Oc1c(C)nc2c(c1Br)cccc2 Request for Quotation
Chemical Name: 3-Quinolinol, 4-bromo-2-methyl-
CAS Number: 13235-12-6
Product Number: AG0010KV(AGN-PC-0JLUER)
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:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
236.979g/mol
Monoisotopic Mass:
236.979g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
188
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


4-Bromo-2-methylquinolin-3-ol (BMQO) is a versatile compound widely utilized in chemical synthesis due to its unique structural properties and reactivity. This derivative of quinoline has proven to be a valuable building block in the development of various pharmaceuticals, agrochemicals, and organic materials.In organic synthesis, BMQO serves as a key intermediate in the production of complex molecules and heterocyclic compounds. Its bromine and hydroxyl functionalities make it a useful reagent for the introduction of specific functional groups through substitution or coupling reactions. BMQO can undergo nucleophilic substitution, electrophilic substitution, and transition metal-catalyzed cross-coupling reactions, enabling the creation of diverse chemical structures.Furthermore, 4-Bromo-2-methylquinolin-3-ol exhibits potential biological activity, making it a promising candidate for drug discovery and development. Its quinoline core is known for its antimicrobial, antiviral, and anticancer properties, which have attracted significant attention in the pharmaceutical industry. By incorporating BMQO as a structural motif in drug design, researchers are able to explore new therapeutic agents with enhanced pharmacological profiles.Overall, the application of 4-Bromo-2-methylquinolin-3-ol in chemical synthesis offers a valuable approach to accessing structurally diverse compounds with potential biological activity. Its versatility and reactivity make it a valuable tool for the creation of novel molecules with applications in various fields of chemistry and pharmaceutical science.