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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(1H)-Quinazolinone, 2-amino-7-bromo-

Brc1ccc2c(c1)nc([nH]c2=O)N Request for Quotation
Chemical Name: 4(1H)-Quinazolinone, 2-amino-7-bromo-
CAS Number: 885277-56-5
Product Number: AG0045VN(AGN-PC-093R1C)
Synonyms:
MDL No:
Molecular Formula: C8H6BrN3O
Molecular Weight: 240.0567

Identification/Properties

Properties
Form:
Solid
Computed Properties
Molecular Weight:
240.06g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
238.969g/mol
Monoisotopic Mass:
238.969g/mol
Topological Polar Surface Area:
67.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
266
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-H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Amino-7-bromoquinazolin-4(3H)-one is a valuable chemical compound widely used in chemical synthesis processes. This versatile building block serves as a key intermediate in the production of various pharmaceuticals and organic compounds. With its unique structural properties, 2-Amino-7-bromoquinazolin-4(3H)-one plays a crucial role in the development of new drugs, agrochemicals, and materials. Its presence in the synthesis pathway enables the formation of complex molecular structures, enhancing the efficiency and diversity of chemical reactions. Overall, the application of 2-Amino-7-bromoquinazolin-4(3H)-one in chemical synthesis demonstrates its significance in advancing research and innovation within the field of chemistry.