Interesting facts
Interesting Facts about 3-Aminonaphthalene-2-carboxylic Acid
3-Aminonaphthalene-2-carboxylic acid is a fascinating compound with a variety of applications in both academic research and industry. Here are some interesting points to consider:
- Structural Significance: This compound is derived from naphthalene, a polycyclic aromatic hydrocarbon. Its structure includes an amino group and a carboxylic acid functional group, making it an example of an amino acid derivative with unique properties.
- Role in Organic Synthesis: 3-Aminonaphthalene-2-carboxylic acid serves as an important building block in the synthesis of dyes, pharmaceuticals, and agrochemicals, showcasing its versatility in organic chemistry.
- Biological Relevance: The incorporation of amino groups into aromatic compounds contributes to biological activity. Some derivatives of this compound have been studied for their potential therapeutic effects, including anti-cancer properties.
- Fluorescent Properties: This compound may exhibit fluorescent behavior, making it valuable in the development of fluorescent probes in biological imaging and materials science.
- Research Applications: In literature, it has been used as a precursor in the preparation of various organic materials, including advanced nanomaterials and polymer systems.
As you explore 3-aminonaphthalene-2-carboxylic acid, remember that its diverse features highlight the beauty of chemistry in designing compounds with a multitude of uses. “Every structure tells a story,” and this compound is no exception, holding the potential for innovation across various scientific fields.
Synonyms
3-AMINO-2-NAPHTHOIC ACID
3-Aminoisonaphthoic acid
2-Amino-3-naphthoic acid
2-Naphthalenecarboxylic acid, 3-amino-
2-Amino-3-carboxynaphthalene
3-Amino-2-naphthalenecarboxylic acid
2-Naphthoic acid, 3-amino-
UNII-IV5Z0PHL5D
IV5Z0PHL5D
EINECS 227-726-2
NSC 37061
BRN 0744099
NSC-37061
3-Amino-2-naphthoric acid
DTXSID8064066
3-14-00-01341 (Beilstein Handbook Reference)
3-AMINO-2-NAPHTHOIC ACID [MI]
DTXCID2042642
227-726-2
xfxolbnqyfrslq-uhfffaoysa-n
5959-52-4
3-aminonaphthalene-2-carboxylic acid
MFCD00004115
beta-Naphthylamine-3-carboxylic Acid
CHEMBL1935084
2-Aminonaphthalene-3-carboxylic acid
3-amino-naphthalene-2-carboxylic acid
3-azanylnaphthalene-2-carboxylic acid
3-amino-2-naphthoic
3-amino-2 napthoic acid
3-amino-2-napthoic acid
3-amino-2-naphthalic acid
Oprea1_749540
WLN: L66J CZ DVQ
BIDD:GT0648
SCHEMBL197490
3-AMINO-2-NAPHTHOICACID
CHEBI:177018
HMS1786G14
3-Amino-2-naphthoic acid technical
NSC37061
BDBM50360482
GEO-00178
STK372686
AKOS000120491
CS-W005148
FA00337
HY-W005148
DS-12509
SY049342
DB-053419
A2258
NS00015134
EN300-17260
F20401
3-Amino-2-naphthoic acid, technical grade, 80%
AO-801/41077418
3-Amino-2-naphthoic acid, technical, >=80% (NT)
Q27280916
Z56899208
F2191-0021
NYE
Solubility of 3-Aminonaphthalene-2-carboxylic Acid
3-Aminonaphthalene-2-carboxylic acid, with the chemical formula C11H11NO2, exhibits interesting properties related to its solubility.
This compound is known for its moderate solubility in water, primarily due to the presence of its carboxylic acid functional group. However, it is significantly more soluble in organic solvents. Here are some key points regarding its solubility:
In summary, while 3-aminonaphthalene-2-carboxylic acid is moderately soluble in water, its solubility profile underscores the importance of selecting the appropriate solvent and the influence of environmental conditions on its behavior. This compound invites curiosity regarding its applications in various chemical processes, particularly in organic synthesis and medicinal chemistry.