Cat. No JK273933_1_G
J&K Chemical

Product Information

Product Name
2-Bromo-5-nitrobenzoic acid, 98%
Brand Name
J&K
Product Number
273933
CAS
943-14-6
Molecular Formula
C7H4BrNO4
Molecular Weight
246.01
SDS Document
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

Properties

Melting Point
180-181

Safety Information

GHS Symbols
Hazard Symbol
Signal Word
Warning
Hazard Statement
H315
H319
H335
Precautionary Statement
P280
P321
P261
P271
P319
P405
P501
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References

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

2-Bromo-5-nitrobenzoic acid, 98%

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