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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-2-chloro-6-methylquinazoline

Cc1cc(Br)c2c(c1)cnc(n2)Cl Request for Quotation
Chemical Name: 8-Bromo-2-chloro-6-methylquinazoline
CAS Number: 1388024-91-6
Product Number: AG0019LK(AGN-PC-0WAHG6)
Synonyms:
MDL No:
Molecular Formula: C9H6BrClN2
Molecular Weight: 257.5143

Identification/Properties

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


8-Bromo-2-chloro-6-methylquinazoline is a versatile chemical compound that finds wide application in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block in the synthesis of various biologically active molecules and complex organic compounds. Its unique structure and reactivity make it a valuable tool for chemists engaged in drug discovery and development.In chemical synthesis, 8-Bromo-2-chloro-6-methylquinazoline can be used as a precursor for the synthesis of diverse quinazoline derivatives, which exhibit a range of biological activities such as anti-cancer, anti-inflammatory, and anti-microbial properties. By incorporating this compound into synthetic pathways, chemists can access a variety of structurally diverse molecules with potential therapeutic applications.Furthermore, the presence of both bromine and chlorine substituents on the quinazoline ring imparts specific reactivity to 8-Bromo-2-chloro-6-methylquinazoline, allowing for selective functionalization at different positions of the molecule. This enables chemists to tailor the structure of the final product to optimize its biological activity or physical properties.Overall, 8-Bromo-2-chloro-6-methylquinazoline is a valuable tool in the toolkit of synthetic chemists, offering versatility and customization in the development of novel compounds for various applications in the field of medicinal and agricultural chemistry. Its strategic incorporation in synthetic routes enables the efficient and controlled synthesis of target molecules with desired properties.