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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)-

Isoquinoline, 5-bromo-8-nitro-

[O-][N+](=O)c1ccc(c2c1cncc2)Br Request for Quotation
Chemical Name: Isoquinoline, 5-bromo-8-nitro-
CAS Number: 63927-23-1
Product Number: AG003MJY(AGN-PC-0JWHRO)
Synonyms:
MDL No:
Molecular Formula: C9H5BrN2O2
Molecular Weight: 253.0522

Identification/Properties

Properties
MP:
136-140 °C
BP:
386.9°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
253.055g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
251.953g/mol
Monoisotopic Mass:
251.953g/mol
Topological Polar Surface Area:
58.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
231
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


5-Bromo-8-nitroisoquinoline is a versatile compound widely used in chemical synthesis due to its unique properties. This molecule serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and organic materials. In organic synthesis, 5-Bromo-8-nitroisoquinoline acts as a valuable intermediate for the preparation of diverse heterocyclic compounds with potential biological activities. Its nitro and bromo functional groups offer opportunities for further derivatization through nucleophilic substitution reactions, allowing chemists to tailor its reactivity for specific synthetic pathways. By incorporating 5-Bromo-8-nitroisoquinoline as a strategic intermediate in their synthetic routes, researchers can access a wide array of structurally diverse molecules with the potential to exhibit interesting pharmacological or material properties.