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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-bromo-1-nitroisoquinoline

[O-][N+](=O)c1ncc(c2c1cccc2)Br Request for Quotation
Chemical Name: 4-bromo-1-nitroisoquinoline
CAS Number: 182184-81-2
Product Number: AG0023GM(AGN-PC-00OOF8)
Synonyms:
MDL No:
Molecular Formula: C9H5BrN2O2
Molecular Weight: 253.0522

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H311-H331
Precautionary Statements:
P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-1-nitroisoquinoline is a versatile chemical compound that finds application in various chemical synthesis processes. Its unique structure and reactivity make it a valuable reagent in the preparation of complex organic molecules. One of the key uses of 4-Bromo-1-nitroisoquinoline is as a precursor for the synthesis of substituted isoquinolines, which are important building blocks in pharmaceutical and agrochemical industries. Additionally, this compound can undergo various transformations such as nucleophilic substitution, reduction, and coupling reactions, enabling the efficient and strategic synthesis of diverse organic compounds. Its ability to participate in these reactions makes 4-Bromo-1-nitroisoquinoline a valuable tool for organic chemists seeking to design and develop novel molecules with desired properties.