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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)-

8-bromo-5-chloroquinoline

Clc1ccc(c2c1cccn2)Br Request for Quotation
Chemical Name: 8-bromo-5-chloroquinoline
CAS Number: 1154741-20-4
Product Number: AG000G0Q(AGN-PC-001RST)
Synonyms:
MDL No:
Molecular Formula: C9H5BrClN
Molecular Weight: 242.4997

Identification/Properties

Computed Properties
Molecular Weight:
242.5g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
240.929g/mol
Monoisotopic Mass:
240.929g/mol
Topological Polar Surface Area:
12.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
165
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


8-Bromo-5-chloroquinoline is a versatile chemical compound that finds widespread applications in chemical synthesis processes. This compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its unique structure and reactivity, 8-Bromo-5-chloroquinoline is particularly useful in the development of novel drug candidates and active ingredients.In chemical synthesis, 8-Bromo-5-chloroquinoline can be utilized as a key intermediate in the preparation of complex organic molecules. Its presence in a synthetic pathway can enable the introduction of specific functional groups or structural motifs that are essential for the desired biological activity or chemical properties of the final product. By incorporating 8-Bromo-5-chloroquinoline into a synthesis scheme, chemists can efficiently access a diverse array of molecular frameworks with strategic precision.Moreover, the selective reactivity of the bromo and chloro substituents in 8-Bromo-5-chloroquinoline allows for strategic modifications and derivatizations to tailor the compound for specific applications. Chemists can leverage these reactive sites to perform cross-coupling reactions, nucleophilic substitutions, and other transformations that enable the fine-tuning of molecular structures. This versatility makes 8-Bromo-5-chloroquinoline a valuable resource in the toolbox of synthetic chemists working on the design and optimization of biologically active compounds and functional molecules.