138724-32-0

Basic information

• Product Name: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)
• Synonyms: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)
• CAS NO: 138724-32-0
• Molecular Formula: C₈H₆F₃NO₂
• Molecular Weight: 205.1339496
• Product Categories: AMINOACID
• Mol File: 138724-32-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(138724-32-0)
• EPA Substance Registry System: Benzoic acid, 4-amino-2,3,5-trifluoro-, methyl ester (9CI)(138724-32-0)

Safety Data

• Hazardous Substances Data: 138724-32-0(Hazardous Substances Data)

Upstream product

• 110-82-7 cyclohexane 
• 138724-31-9 Methyl 4-Azido-3,5,6-trifluorobenzoate 
• 109-89-7 diethylamine 
• 1201-31-6 2,3,4,5-tetrafluorobenzoic acid 
• 5292-42-2 methyl-2,3,4,5-tetrafluoro benzoate 
• 126695-64-5 methyl 2-amino-4-azido-3,5,6-trifluorobenzoate 
• 715-37-7 methyl 4-amino-2,3,5,6-tetrafluorobenzoate 
• 602-94-8 Pentafluorobenzoic acid 
• 36629-42-2 methyl pentafluorobenzoate 
• 122590-75-4 methyl 4-azidotetrafluorobenzoate 

Downstream Products

• 122033-75-4 4-amino-2,3,5-trifluorobenzoic acid 
• 122033-62-9 4-bromo-2,3,5-trifluorobenzoic acid 

Relevant articles and documents

FUSED TRICYCLIC COMPOUNDS USEFUL AS ANTICANCER AGENTS

The specification relates to compounds of Formula (A) and pharmaceutically acceptable salts thereof. The specification also relates to processes and intermediates used for their preparation, pharmaceutical compositions containing them and their use in the treatment of cell proliferative disorders.

Toward the Development of Radiolabeled Fluorophenyl Azide-Based Photolabeling Reagents: Synthesis and Photolysis of Iodinated 4-Azidoperfluorobenzoates and 4-Azido-3,5,6-trifluorobenzoates

Two approaches for the incorporation of iodine into funtionalized perfluorophenyl azides (PFPAs) were demonstrated by the synthesis of 3, 5, and 8, with the azido and iodo groups in the same aryl ring, and 14 and 15, with the azido and iodo groups in diff