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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-1,2-dihydroisoqunolin-3(4H)-one

Brc1cc2CC(=O)NCc2cc1 Request for Quotation
Chemical Name: 6-Bromo-1,2-dihydroisoqunolin-3(4H)-one
CAS Number: 943749-57-3
Product Number: AG019ENQ(AGN-PC-0W40AX)
Synonyms:
MDL No:
Molecular Formula: C9H8BrNO
Molecular Weight: 226.0699

Identification/Properties

Computed Properties
Molecular Weight:
226.073g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
224.979g/mol
Monoisotopic Mass:
224.979g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
195
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-1,2-dihydroisoquinolin-3(4H)-one is a valuable chemical intermediate widely utilized in organic synthesis. This compound plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials due to its unique structure and reactivity. Its distinct bromo group allows for selective functionalization, making it an excellent building block in the construction of complex molecular structures. In addition, 6-Bromo-1,2-dihydroisoquinolin-3(4H)-one serves as a key starting material in the synthesis of bioactive compounds, such as kinase inhibitors and natural product derivatives. Its versatility and synthetic utility make it a versatile tool for chemists seeking to access diverse molecular architectures efficiently and selectively.