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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-methoxyquinazoline

COc1cc(Br)cc2c1nc(Cl)nc2 Request for Quotation
Chemical Name: 6-bromo-2-chloro-8-methoxyquinazoline
CAS Number: 953039-14-0
Product Number: AG0065O3(AGN-PC-07XTJ9)
Synonyms:
MDL No:
Molecular Formula: C9H6BrClN2O
Molecular Weight: 273.5137

Identification/Properties

Properties
BP:
342.1±35.0 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
273.514g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
271.935g/mol
Monoisotopic Mass:
271.935g/mol
Topological Polar Surface Area:
35A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
207
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#:
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


6-Bromo-2-chloro-8-methoxyquinazoline is a versatile compound widely employed in chemical synthesis as a key building block in the development of various pharmaceuticals, agrochemicals, and functional organic materials. This compound serves as a valuable intermediate in the synthesis of more complex molecules due to its unique structural features and reactivity. With its strategic positioning of bromine, chlorine, and methoxy functional groups on the quinazoline ring, 6-Bromo-2-chloro-8-methoxyquinazoline offers diverse synthetic pathways for the modification and elaboration of its structure to access a wide range of derivatives with tailored properties. Its versatile nature makes it a valuable tool for medicinal chemists, enabling the design and synthesis of novel drug candidates with enhanced biological activities. Furthermore, its utility extends to the development of new materials with specialized functions, highlighting its importance in advancing the field of chemical synthesis.