1. Home
  2. 2-bromo-1-oxidopyridin-1-ium;hydrobromide

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

2-bromo-1-oxidopyridin-1-ium;hydrobromide

Brc1cccc[n+]1[O-].Br Request for Quotation
Chemical Name: 2-bromo-1-oxidopyridin-1-ium;hydrobromide
CAS Number: 206860-49-3
Product Number: AG002IQE(AGN-PC-0KK07D)
Synonyms:
MDL No:
Molecular Formula: C5H5Br2NO
Molecular Weight: 254.9073

Identification/Properties

Computed Properties
Molecular Weight:
254.909g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
254.872g/mol
Monoisotopic Mass:
252.874g/mol
Topological Polar Surface Area:
25.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
78.8
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-Bromopyridine 1-oxide hydrobromide is a versatile chemical compound widely used in chemical synthesis as a key building block in various reactions. This compound plays a crucial role in the preparation of complex organic molecules and pharmaceutical intermediates due to its unique chemical properties.One of the primary applications of 2-Bromopyridine 1-oxide hydrobromide is in the synthesis of heterocyclic compounds. It can participate in a variety of chemical transformations such as nucleophilic aromatic substitution reactions, palladium-catalyzed cross-coupling reactions, and radical reactions. These reactions enable the formation of new carbon-carbon and carbon-heteroatom bonds, allowing for the creation of diverse chemical structures.Furthermore, 2-Bromopyridine 1-oxide hydrobromide is often employed as a reagent in the functionalization of aromatic compounds. Its ability to introduce the bromo-oxide group into organic molecules makes it a valuable tool for modifying the properties of various substrates. This compound can also serve as a precursor for the synthesis of other functionalized heterocycles, providing access to a wide range of chemical scaffolds with potential biological activities.In summary, 2-Bromopyridine 1-oxide hydrobromide is a crucial component in the toolbox of synthetic chemists for the construction of complex organic molecules and the development of novel chemical entities with diverse applications. Its versatility and utility in chemical synthesis make it an indispensable reagent for the preparation of advanced materials and pharmaceutical compounds.