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Sku CI27957_1_G
Chem Impex
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Product Information

Product Name
2-Bromo-5-nitrobenzoic acid
Brand Name
Chem Impex
Product Number
27957
CAS
943-14-6
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
243025
IUPAC Name
2-bromo-5-nitrobenzoic acid
InChI Key
UVFWYVCDRKRAJH-UHFFFAOYSA-N
SMILES
C1=CC(=C(C=C1N+(=O)O-)C(=O)O)Br

Application

2-Bromo-5-nitrobenzoic acid is widely utilized in research focused on:

Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the production of various pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs.

Organic Synthesis: It is commonly used in organic chemistry for the synthesis of complex molecules, allowing researchers to create new compounds with desired properties.

Biochemical Research: The compound is employed in studies involving enzyme inhibition, helping researchers understand biochemical pathways and develop potential therapeutic agents.

Material Science: It finds applications in the development of novel materials, including polymers and coatings, due to its unique chemical properties that enhance material performance.

Analytical Chemistry: 2-Bromo-5-nitrobenzoic acid is used as a reagent in various analytical techniques, aiding in the detection and quantification of other chemical substances.

References Data Source From Pubchem

Synthesis and antitumor activities of 3-substituted-analine derivatives: structure modifications of Tuv part of tubulysins

Publication Name: Chemistry Central Journal
Publication Date: 2018-11-15
DOI: 10.1186/s13065-018-0483-5

Enzymatic hydrolysis by transition-metal dependent nucleophilic aromatic substitution.

Publication Name: Nature Chemical Biology
Publication Date: 2016-10-03
DOI: 10.1038/nchembio.2191

An efficient synthesis of isocoumarins via a CuI catalyzed cascade reaction process

Publication Name: Science in China Series B: Chemistry
Publication Date: 2009-10-18
DOI: 10.1007/s11426-009-0197-6

Diastereo- and Enantioselective Hydrogenative Aldol Coupling of Vinyl Ketones: Design of Effective Monodentate TADDOL-Like Phosphonite Ligands

Publication Name: Journal of the American Chemical Society
Publication Date: 2008-02-12
DOI: 10.1021/ja710862u

Regioselective Copper-Catalyzed C–N and C–S Bond Formation Using Amines, Thiols and Halobenzoic Acids

Publication Name: Synthesis
Publication Date: 2007-11-16
DOI: 10.1055/s-2007-990875