Interesting facts
Interesting Facts about 2-Anilinobenzoic Acid
2-Anilinobenzoic acid, a novel aromatic compound, showcases a fascinating integration of both aniline and benzoic acid structures. This compound is noteworthy for several reasons:
- Unique Structure: The presence of both an amine group and a carboxylic acid group in its structure makes it a valuable compound in the field of organic chemistry.
- Applications in Medicine: Due to its biological activity, 2-anilinobenzoic acid has been studied for potential medicinal applications, particularly as a pharmacologically active agent.
- Aromaticity: The compound contains aromatic rings that contribute to its stability and reactivity. The delocalization of electrons in these rings is a key feature that scientists find intriguing.
- Intermolecular Interactions: The compound exhibits interesting hydrogen bonding behavior, particularly due to its carboxylic acid group, which has implications in both synthetic and biological chemistry.
- Dyes and Pigments: Compounds similar to 2-anilinobenzoic acid are often explored for their potential in creating dyes or pigments, showcasing the versatility of such aromatic structures.
As a scientist or chemistry student, one might appreciate how 2-anilinobenzoic acid serves as a stepping stone into the broader world of organic compounds and their multifaceted applications. Its combination of simple organic chemistry with real-world applications makes it an exciting topic of study.
Synonyms
N-phenylanthranilic acid
91-40-7
Fenamic acid
2-(Phenylamino)benzoic acid
2-Anilinobenzoic acid
Diphenylamine-2-carboxylic acid
Phenylanthranilic acid
Benzoic acid, 2-(phenylamino)-
2-Carboxydiphenylamine
o-Anilinobenzoic acid
N-Phenyl-o-aminobenzoic acid
Anthranilic acid, N-phenyl-
N-Phenyl-2-aminobenzoic acid
2-Phenylamino-benzoic acid
MFCD00002421
NSC 215211
EINECS 202-066-8
N-Phenylanthranilic
BRN 1456607
952VN06WBB
CHEBI:34756
AI3-08880
ortho-anilinobenzoic acid
2-phenylazanylbenzoic acid
NSC-215211
CHEMBL23832
DTXSID6059025
N-phenyl-ortho-aminobenzoic acid
N-PHENYLANTHRANILIC ACID [MI]
diphenylamine carboxylate
diphenylamine-2-carboxylate
SR-01000075342
n-phenyl anthranilic acid
UNII-952VN06WBB
oAnilinobenzoic acid
2Anilinobenzoic acid
2Carboxydiphenylamine
NPhenylanthranilic acid
2-anilino-benzoic acid
NPhenyloaminobenzoic acid
N-phenyl-anthranilic acid
Anthranilic acid, Nphenyl
benzoic acid, 2-anilino-
2(Phenylamino)benzoic acid
Lopac-144509
o-(Phenylamino)benzoic acid
PhenylanthranilsA currencyure
Diphenylamine2carboxylic acid
CBiol_001836
Lopac0_000011
Oprea1_414882
Oprea1_622264
SCHEMBL25828
BSPBio_001421
CBDivE_001949
KBioGR_000141
KBioGR_002302
KBioSS_000141
KBioSS_002304
MLS002153472
Benzoic acid, 2(phenylamino)
BIDD:GT0820
SPECTRUM1505156
GTPL4182
N-Phenylanthranilic acid, 98%
DTXCID0048717
BCBcMAP01_000076
Diphenylaminecarboxylic acid-(2)
KBio2_000141
KBio2_002302
KBio2_002709
KBio2_004870
KBio2_005277
KBio2_007438
KBio3_000281
KBio3_000282
KBio3_002782
ZWJINEZUASEZBH-UHFFFAOYSA-
NSC4273
cMAP_000012
Bio1_000122
Bio1_000611
Bio1_001100
Bio2_000141
Bio2_000621
HMS1361H03
HMS1791H03
HMS1989H03
HMS2232G15
HMS3260C03
HMS3373F04
HMS3402H03
NSC-4273
Tox21_500011
BBL008122
BDBM50337278
NSC215211
s5517
STK089446
Diphenylamine-2-carboxylic acid; DPC
AKOS000118791
CCG-204107
CS-W021005
FP71363
HY-W040265
LP00011
SB78726
SDCCGMLS-0412242.P028
SDCCGSBI-0050000.P002
IDI1_033891
MLS-0412242
NCGC00014989-01
NCGC00014989-02
NCGC00014989-03
NCGC00014989-04
NCGC00014989-05
NCGC00014989-06
NCGC00014989-07
NCGC00014989-08
NCGC00014989-12
NCGC00093536-01
NCGC00093536-02
NCGC00093536-03
NCGC00093536-04
NCGC00093536-05
NCGC00093536-06
NCGC00260696-01
DS-14719
SMR001230825
SY048561
MLS-0412242.P016
DB-057256
D0873
EU-0100011
NS00007989
EN300-18386
D70372
AE-641/02494034
N-Phenylanthranilic acid, technical, >=95% (T)
Q498436
SR-01000075342-1
SR-01000075342-2
BRD-K80863915-001-02-9
BRD-K80863915-001-05-2
Z57127451
F3145-3322
202-066-8
InChI=1/C13H11NO2/c15-13(16)11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,14H,(H,15,16)
Solubility of 2-Anilinobenzoic Acid (C13H11NO2)
2-Anilinobenzoic acid, a compound with both an amine and a carboxylic acid functional group, exhibits unique solubility characteristics. When considering its solubility in various solvents, it is important to note the following:
In summary, the solubility of 2-anilinobenzoic acid is significantly influenced by the solvent's polarity and temperature conditions. As a result, one might say:
This quote underscores the importance of considering both the chemical structure and the environment when examining the solubility of compounds like 2-anilinobenzoic acid.