Interesting facts
Interesting Facts about 2-[3-(Trifluoromethyl)anilino]benzoic Acid
2-[3-(Trifluoromethyl)anilino]benzoic acid is a fascinating compound with various applications in the field of chemistry and beyond. Here are some intriguing aspects of this compound:
- Structure and Properties: This compound features a unique arrangement of atoms that includes a trifluoromethyl group, which significantly influences its chemical properties and reactivity.
- Biological Activity: Certain derivatives of benzoic acids, including this compound, are known for their biological activities. They may exhibit potential as pharmaceuticals or agrochemicals due to their ability to interact with biological systems.
- Applications in Synthesis: The incorporation of fluorinated groups is a common strategy in organic synthesis. This compound can serve as an important intermediate in the synthesis of more complex molecules.
- Environmental Impact: Compounds containing fluorine, particularly trifluoromethyl groups, can have unique environmental and ecological effects. Understanding these interactions is crucial for evaluating their safety and sustainability.
- Chemical Reactions: 2-[3-(Trifluoromethyl)anilino]benzoic acid can participate in various chemical reactions, making it a valuable compound for researchers studying reaction mechanisms and developing new materials.
As a compound of interest, 2-[3-(trifluoromethyl)anilino]benzoic acid highlights the intricate relationship between organic chemistry and its applications in diverse fields. The study of such compounds opens avenues for innovations and contributes to our understanding of chemical interactions in nature. As chemists, we must approach these compounds with curiosity and consideration for their broader impacts.
Synonyms
flufenamic acid
530-78-9
Arlef
Fluphenamic acid
Nichisedan
Achless
Acido flufenamico
N-(3-Trifluoromethylphenyl)anthranilic acid
Flufacid
Fullsafe
Plostene
Tecramine
Lanceat
Paraflu
Parlef
Parlif
Surika
Flufenaminsaeure
2-((3-(Trifluoromethyl)phenyl)amino)benzoic acid
Reumajust A
Ansatin
Meralen
Ristogen
Sastridex
2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid
Fluore-200
Acide flufenamique
CI 440
NSC-82699
ANT-1
Acidum flufenamicum
CN-27,554
3'-Trifluoromethyldiphenylamine-2-carboxylic acid
2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid
TVX 916
INF 1837
Benzoic acid, 2-[[3-(trifluoromethyl)phenyl]amino]-
Flufenaminsaeure [German]
Acido flufenamico [Italian]
C.I. 440
INF-1837
CCRIS 5266
NSC 219007
Acide flufenamique [INN-French]
Acido flufenamico [INN-Spanish]
Acidum flufenamicum [INN-Latin]
2-[3-(Trifluoromethyl)anilino]benzoic acid
Benzoic acid, 2-((3-(trifluoromethyl)phenyl)amino)-
EINECS 208-494-1
60GCX7Y6BH
N-(alpha,alpha,alpha-Trifluoro-m-tolyl)anthranilic acid
2-((3-Trifluromethyl)phenyl)aminobenzoic acid
2-[[3-(TRIFLUOROMETHYL)PHENYL]AMINO] BENZOIC ACID
Flufenamic acid [USAN:INN:BAN:JAN]
NSC-219007
N-(m-Trifluoromethylphenyl)-2-aminobenzoic acid
BRN 1996069
Arlef (TN)
DTXSID7023063
CHEBI:42638
CI-440
2-(3-Trifluoromethylanilino)benzoic Acid
CN-27554
FLUFENAMIC ACID [MI]
CHEMBL23588
FLUFENAMIC ACID [INN]
FLUFENAMIC ACID [JAN]
FLUFENAMIC ACID [USAN]
MLS000028563
DTXCID303063
FLUFENAMIC ACID [MART.]
N-(3-Trifluoromethylphenyl)-anthranilic acid
N-[3-(Trifluoromethyl)phenyl]anthranilic acid
FLUFENAMIC ACID [WHO-DD]
EC 208-494-1
Saal-F
3-14-00-00905 (Beilstein Handbook Reference)
NCGC00016490-06
Anthranilic acid, N-(alpha,alpha,alpha-trifluoro-m-tolyl)-
CAS-530-78-9
CN-27544
SMR000059027
N-(.alpha.,.alpha.,.alpha.-Trifluoro-m-tolyl)anthranilic acid
WLN: QVR BMR CXFFF
FFA
N-((m-Trifluoromethyl)phenyl)-2-aminobenzoic acid
FLUFENAMIC ACID (MART.)
Acide flufenamique (INN-French)
Acido flufenamico (INN-Spanish)
Acidum flufenamicum (INN-Latin)
Flufenamicacid
Anthranilic acid, N-(.alpha.,.alpha.,.alpha.-trifluoro-m-tolyl)-
Acid, Flufenamic
FLF
2-(3-(trifluoromethyl)anilino)benzoic acid
2-[(3-Trifluromethyl)phenyl]aminobenzoic acid
N-[(3-Trifluoromethyl)phenyl]anthranilic acid
N-[(m-Trifluoromethyl)phenyl]-2-aminobenzoic acid
N-[m-(Trifluoromethyl)phenyl]-2-aminobenzoic acid
SR-01000000241
Anthranilic acid,.alpha.,.alpha.-trifluoro-m-tolyl)-
N-(.alpha.,.alpha.-Trifluoro-m-tolyl)anthranilic acid
UNII-60GCX7Y6BH
2-((3-(TRIFLUOROMETHYL)PHENYL)AMINO) BENZOIC ACID
flufenamic-acid
Prestwick_220
MFCD00002422
Spectrum_001257
1bm7
Opera_ID_578
flufenamic acid aluminium
Prestwick0_000203
Prestwick1_000203
Prestwick2_000203
Prestwick3_000203
Spectrum2_000789
Spectrum3_001273
Spectrum4_000102
Spectrum5_000686
Flufenamic acid (Standard)
CBiol_001756
SCHEMBL17497
BSPBio_000185
BSPBio_001319
BSPBio_002866
CBDivE_012649
KBioGR_000039
KBioGR_000424
KBioGR_002267
KBioSS_000039
KBioSS_001737
KBioSS_002268
MLS001148610
DivK1c_000581
SPECTRUM1501015
SPBio_000898
SPBio_002106
BPBio1_000205
GTPL2447
BCBcMAP01_000039
BDBM17636
HMS501N03
HY-B1221R
KBio1_000581
KBio2_000039
KBio2_001737
KBio2_002267
KBio2_002607
KBio2_004305
KBio2_004835
KBio2_005175
KBio2_006873
KBio2_007403
KBio3_000077
KBio3_000078
KBio3_002366
KBio3_002747
M01AG03
cMAP_000004
NINDS_000581
Bio1_000042
Bio1_000531
Bio1_001020
Bio2_000039
Bio2_000519
Flufenamic acid (JAN/USAN/INN)
GLXC-27023
HMS1361B21
HMS1568J07
HMS1791B21
HMS1921B21
HMS1989B21
HMS2089E07
HMS2092B09
HMS2095J07
HMS2232G24
HMS3371F01
HMS3402B21
HMS3652F06
HMS3712J07
HMS3885P15
Pharmakon1600-01501015
HY-B1221
NSC82699
Tox21_110452
Tox21_302111
CCG-40167
NSC219007
NSC757823
s4268
STK985630
AKOS000265536
Tox21_110452_1
CS-4811
DB02266
FF23323
KS-1143
NSC-757823
IDI1_000581
IDI1_033789
NCGC00016490-01
NCGC00016490-02
NCGC00016490-03
NCGC00016490-04
NCGC00016490-05
NCGC00016490-07
NCGC00016490-08
NCGC00016490-09
NCGC00016490-10
NCGC00016490-12
NCGC00023200-03
NCGC00023200-04
NCGC00023200-05
NCGC00023200-06
NCGC00023200-07
NCGC00255175-01
SBI-0051633.P002
DB-052254
2-[3-(trifluoromethyl)anilino]-benzoic acid
AB00052198
ETOFENAMATE IMPURITY A [EP IMPURITY]
n-(a,a,a-trifluoro-m-tolyl)anthranilic acid
NS00000475
SW196528-3
T2354
UNM000001246003
2-[3-(Trifluoromethyl)anilino]benzoic acid #
EN300-16858
2-(3-(trifluoromethyl)phenylamino)benzoic acid
2-[(3-Trifluoromethylphenyl)amino]benzoic Acid
D01581
D97458
AB00052198-14
AB00052198_15
Q416341
SR-01000000241-2
SR-01000000241-3
BRD-K44067360-001-06-3
BRD-K44067360-001-16-2
BRD-K44067360-001-29-5
BRD-K44067360-001-30-3
Z56797275
F0909-0007
Flufenamic acid, analytical standard, for drug analysis
2-[[3-(Trifluoromethyl)phenyl]amino]benzoic acid;2-[3-(Trifluoromethyl)anilino]benzoic acid;3'-Trifluoromethyldiphenylamine-2-carbox ylic acid
208-494-1
FFA, Flufenamic acid, 3-[(2-Carboxyphenyl)amino]benzotrifluoride, 2-Carboxy-3'-(trifluoromethyl)diphenylamine
Solubility of 2-[3-(trifluoromethyl)anilino]benzoic acid (C14H10F3NO2)
The solubility of 2-[3-(trifluoromethyl)anilino]benzoic acid is influenced by its molecular structure, which presents a unique combination of functional groups. Here are some key points regarding its solubility:
In summary, the solubility behavior of 2-[3-(trifluoromethyl)anilino]benzoic acid is a complex interplay of its functional groups. As stated, "it is important to consider both hydrophilic and hydrophobic interactions in order to predict solubility accurately." The compound's solubility profile is likely to vary significantly between different solvents and conditions.