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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)-

4-(bromomethyl)quinoline;hydrobromide

BrCc1ccnc2c1cccc2.Br Request for Quotation
Chemical Name: 4-(bromomethyl)quinoline;hydrobromide
CAS Number: 73870-28-7
Product Number: AG005W6X(AGN-PC-09RRFK)
Synonyms:
MDL No:
Molecular Formula: C10H9Br2N
Molecular Weight: 302.9932

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
302.997g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
302.908g/mol
Monoisotopic Mass:
300.91g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
149
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:
2
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-(Bromomethyl)quinoline hydrobromide is a versatile chemical compound that finds wide application in chemical synthesis processes. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and structural properties.One primary application of 4-(Bromomethyl)quinoline hydrobromide is in the field of medicinal chemistry, where it is utilized in the preparation of potential drug candidates. The bromomethyl group in the quinoline ring provides a convenient handle for further functionalization, allowing chemists to introduce specific molecular modifications to enhance the biological activity or pharmacokinetic profile of the final compound.Additionally, this compound is employed in the synthesis of ligands for transition metal catalysis, enabling the development of novel catalyst systems for organic transformations. The presence of the bromide moiety in the quinoline scaffold facilitates cross-coupling reactions, a powerful tool in modern organic chemistry for the formation of carbon-carbon and carbon-heteroatom bonds.Moreover, 4-(Bromomethyl)quinoline hydrobromide plays a crucial role in material science applications, contributing to the preparation of advanced materials with tailored properties. By incorporating this compound into polymer matrices or surface coatings, researchers can modulate the surface reactivity, adhesion properties, or optical characteristics of the resulting materials, opening up new possibilities for various industrial applications.Overall, the unique reactivity and versatile applications of 4-(Bromomethyl)quinoline hydrobromide make it a valuable reagent in the toolkit of synthetic chemists, enabling the synthesis of diverse molecules with important implications in drug discovery, catalysis, and materials science.