Interesting facts
Interesting Facts about 2-amino-5-nitro-benzoic acid
2-amino-5-nitro-benzoic acid, commonly referred to as 5-nitro-2-aminobenzoic acid, is a fascinating compound that belongs to the class of aminobenzoic acids. This compound presents a unique structure that allows it to play significant roles in various applications. Here are some intriguing aspects:
- Dual Functional Groups: The presence of both an amino group (–NH2) and a nitro group (–NO2) in its structure makes it a versatile molecule. These groups can participate in various chemical reactions, promoting its utility in synthetic organic chemistry.
- Pharmaceutical Applications: Due to its structure, 2-amino-5-nitro-benzoic acid is often found in studies relating to anti-inflammatory and analgesic agents. Researchers are continually exploring its potential as a precursor for synthesizing other biologically active compounds.
- Colorimetric Assays: This compound is also utilized in colorimetric assays due to its distinct absorption characteristics. The nitro group in the molecule contributes to its ability to act as a chromophore, making it useful in analytical chemistry.
- Environmental Impact: As a nitro-substituted compound, it is essential to consider the environmental effects of 2-amino-5-nitro-benzoic acid, especially in its degradation products. Understanding how it behaves in natural ecosystems is crucial for evaluating its safety profile.
- Synthetic Routes: Chemists have developed various synthetic pathways to produce this compound, including nitration of amino-substituted benzoic acids. Exploring these routes can offer insights into reaction mechanisms and the stability of functional groups.
Overall, 2-amino-5-nitro-benzoic acid stands out not only for its unique chemical properties but also for its vast implications in chemical research and industrial applications. As scientists continue to investigate its capabilities, this compound may unveil even more fascinating facets in the world of chemistry.
Synonyms
2-AMINO-5-NITROBENZOIC ACID
616-79-5
5-Nitroanthranilic acid
Benzoic acid, 2-amino-5-nitro-
Anthranilic acid, 5-nitro-
1-amino-2-carboxy-4-nitrobenzene
CHEBI:61280
5-Nitroantranilic acid
EINECS 210-493-6
NSC 16208
NSC 63867
DTXSID8060668
DTXCID2043086
Anthranilic acid, 5-nitro-(8CI)
210-493-6
inchi=1/c7h6n2o4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3h,8h2,(h,10,11
ruchwtkmowxhlu-uhfffaoysa-n
2-Amino-5-nitro-benzoic acid
5NAA
MFCD00017039
2-Amino-5-nitrobenzoicacid
5-nitro-anthranilic acid
Cambridge id 5161184
NCIOpen2_000213
CHEMBL39476
SCHEMBL377824
2-azanyl-5-nitro-benzoic acid
BCP19327
HY-Y1681
NSC16208
NSC63867
STR03468
2-Amino-5-nitrobenzoic acid, 95%
BBL000333
NSC-16208
NSC-63867
STK267557
AKOS000120536
AKOS040744422
AC-7405
CS-W020043
FA38393
NCGC00336357-01
BP-20119
SY006070
DB-024171
N0644
NS00034763
EN300-17935
C19788
N60015
AB01330342-02
AG-205/04762061
Q27130976
Z57124408
F0211-0001
6R6
Solubility of 2-amino-5-nitro-benzoic acid
2-amino-5-nitro-benzoic acid (C7H6N2O4) exhibits interesting solubility characteristics, which can be valuable in various applications. Here are some key points regarding its solubility:
Overall, the solubility of 2-amino-5-nitro-benzoic acid is dictated by its molecular structure and environmental conditions, making it suitable for a variety of chemical processes. Its polar nature, coupled with functional group interactions, underscores its significance in synthetic and analytical chemistry.