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Assay
97%
form
solid
mp
172-176 °C (lit.)
SMILES string
OC(=O)c1ccc(F)cc1Br
InChI
1S/C7H4BrFO2/c8-6-3-4(9)1-2-5(6)7(10)11/h1-3H,(H,10,11)
InChI key
RRKPMLZRLKTDQV-UHFFFAOYSA-N
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General description
Amination of 2-bromo-4-fluorobenzoic acid with aniline is reported to yield N-phenyl-4-fluoro-anthranilic acid.
Application
2-Bromo-4-fluorobenzoic acid may be used in the synthesis of:
- 3-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-fluoro-8-(methylthio)dibenzo[b,f]thiepin-10(11H)-one
- 2-((2-carboxy-5-fluorophenyl)amino)-3-methoxybenzoic acid
- 2-bromo-4-fluorobenzamide
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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A chemo- and regioselective copper-catalyzed cross-coupling procedure for amination of 2-bromobenzoic acids is described. The method eliminates the need for acid protection and produces N-aryl and N-alkyl anthranilic acid derivatives in up to 99% yield. N-(1-Pyrene)anthranilic acid has been employed
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