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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-chloro-5-fluoroquinazoline

Fc1cccc2c1c(Cl)ncn2 Request for Quotation
Chemical Name: 4-chloro-5-fluoroquinazoline
CAS Number: 16499-60-8
Product Number: AG00HZ44(AGN-PC-00J205)
Synonyms:
MDL No:
Molecular Formula: C8H4ClFN2
Molecular Weight: 182.5822

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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


4-Chloro-5-fluoroquinazoline, with its unique molecular structure, plays a crucial role in chemical synthesis processes. This compound serves as a versatile building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Through its reactivity and functional groups, 4-Chloro-5-fluoroquinazoline enables the creation of novel compounds with enhanced biological activities and properties. Furthermore, its inclusion in synthetic pathways facilitates the production of complex organic molecules with tailored structures and functionalities, making it a valuable tool for chemists working in various fields of research and development.