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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)-

8-BROMO-1,2-DIHYDROISOQUINOLIN-3(4H)-ONE

O=C1NCc2c(C1)cccc2Br Request for Quotation
Chemical Name: 8-BROMO-1,2-DIHYDROISOQUINOLIN-3(4H)-ONE
CAS Number: 943749-58-4
Product Number: AG00LIJD(AGN-PC-0WAKXP)
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

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


8-Bromo-1,4-dihydro-3(2H)-isoquinolinone serves as a valuable building block in chemical synthesis processes. Due to its unique structural properties, this compound is utilized as a key intermediate in the development of various organic molecules and pharmaceutical compounds. Its incorporation into synthetic pathways enables the efficient construction of complex structures, making it an essential component in the synthesis of diverse chemical products. Moreover, the presence of the bromine functional group enhances the reactivity and versatility of this compound, allowing for precise modifications and derivatization to tailor the desired chemical properties.