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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)-

6-bromo-2-chloro-8-fluoroquinazoline

Brc1cc(F)c2c(c1)cnc(n2)Cl Request for Quotation
Chemical Name: 6-bromo-2-chloro-8-fluoroquinazoline
CAS Number: 953039-25-3
Product Number: AG00IIYV(AGN-PC-0CSNJ7)
Synonyms:
MDL No:
Molecular Formula: C8H3BrClFN2
Molecular Weight: 261.4782232

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-2-chloro-8-fluoroquinazoline is a versatile compound widely used in chemical synthesis processes. This specific quinazoline derivative serves as a valuable building block in the pharmaceutical industry for the development of various drug molecules. Due to its unique structural properties, 6-Bromo-2-chloro-8-fluoroquinazoline can be efficiently utilized in the synthesis of biologically active compounds and potential pharmaceutical agents.In chemical synthesis, this compound acts as a key intermediate for the creation of diverse molecular structures. Its bromo, chloro, and fluoro functional groups make it a valuable substrate for further derivatization and modification, allowing chemists to fine-tune the properties of the target molecules. The presence of these specific functional groups enables chemists to introduce a range of other substituents, facilitating the synthesis of novel compounds with enhanced biological activities.Moreover, the strategic placement of these halogen atoms in the quinazoline scaffold contributes to the compound's reactivity and potential pharmacological properties. By incorporating 6-Bromo-2-chloro-8-fluoroquinazoline into synthetic routes, researchers can access a plethora of structurally diverse molecules with desired pharmacological profiles. Overall, the application of 6-Bromo-2-chloro-8-fluoroquinazoline in chemical synthesis plays a crucial role in the development of new drug candidates and offers promising avenues for drug discovery efforts in the pharmaceutical industry.