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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)-

5-bromo-8-chloroquinoline

Brc1ccc(c2c1cccn2)Cl Request for Quotation
Chemical Name: 5-bromo-8-chloroquinoline
CAS Number: 927800-41-7
Product Number: AG00H0DH(AGN-PC-01LRAD)
Synonyms:
MDL No:
Molecular Formula: C9H5BrClN
Molecular Weight: 242.4997

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-8-chloroquinoline is a versatile chemical compound commonly used in chemical synthesis due to its unique properties and reactivity. This heterocyclic organic compound serves as a valuable building block in the creation of pharmaceuticals, agrochemicals, and materials science.In the field of medicinal chemistry, 5-Bromo-8-chloroquinoline is often employed as a key intermediate in the synthesis of various biologically active compounds. Its functional groups provide opportunities for further modification, allowing chemists to fine-tune the properties of the final product for specific pharmacological purposes. This compound has shown promise in the development of new drugs for a range of therapeutic applications.Additionally, 5-Bromo-8-chloroquinoline plays a crucial role in the synthesis of pesticides and herbicides. By incorporating this compound into the molecular structure of agricultural chemicals, researchers can enhance their efficacy and environmental safety. The unique reactivity of 5-Bromo-8-chloroquinoline enables the construction of complex molecules with improved selectivity and performance in pest control and crop protection.Moreover, in materials science, 5-Bromo-8-chloroquinoline serves as a valuable precursor for the fabrication of advanced materials with tailored properties. Through controlled chemical reactions and functional group transformations, this compound can be incorporated into polymers, coatings, and other high-performance materials. The resulting materials exhibit enhanced characteristics such as durability, conductivity, or optical properties, making them suitable for a wide range of industrial applications.Overall, 5-Bromo-8-chloroquinoline holds significant potential as a versatile tool in chemical synthesis, offering opportunities for innovation and discovery across various scientific disciplines. Its versatility and reactivity make it a valuable ingredient for researchers and chemists striving to develop novel compounds with specific functionalities and applications.