Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
38280
CAS Number:
530-78-9
N-(3-Trifluoromethylphenyl)anthranilic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2-[(3-Trifluoromethylphenyl)amino]benzoic acid, 2-(3-Trifluoromethylanilino)benzoic acid
Hazmat
Documents
$46.77 /25G
Pack Size Availability Price
Request Bulk Quote
Product Information
Synonyms
2-[(3-Trifluoromethylphenyl)amino]benzoic acid, 2-(3-Trifluoromethylanilino)benzoic acid
CAS Number
530-78-9
Purity
≥ 98% (HPLC)
Molecular Formula
C14H10F3NO2
Molecular Weight
0
MDL Number
MFCD00002422
PubChem ID
3371
Melting Point
133 - 137 °C
Appearance
White to almost white powder to crystal
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2-[(3-Trifluoromethylphenyl)amino]benzoic acid, 2-(3-Trifluoromethylanilino)benzoic acid
CAS Number
530-78-9
Purity
≥ 98% (HPLC)
Molecular Formula
C14H10F3NO2
Molecular Weight
0
MDL Number
MFCD00002422
PubChem ID
3371
Melting Point
133 - 137 °C
Appearance
White to almost white powder to crystal
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(3-Trifluoromethylphenyl)anthranilic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting inflammatory diseases and pain management.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, providing effective solutions for pest control while minimizing environmental impact.
  • Material Science: The compound is explored for its potential in developing advanced materials, such as polymers with enhanced thermal and chemical resistance.
  • Analytical Chemistry: It acts as a reagent in analytical methods, aiding in the detection and quantification of other chemical substances in complex mixtures.
  • Research on Fluorinated Compounds: Its unique trifluoromethyl group makes it valuable in studies investigating the properties and applications of fluorinated organic compounds, which often exhibit improved stability and bioactivity.

Citations