CAS 56741-33-4

5-amino-2-fluorobenzoic acid

Description:

5-Amino-2-fluorobenzoic acid is an aromatic amino acid derivative characterized by the presence of both an amino group (-NH2) and a fluorine atom attached to a benzoic acid structure. This compound features a fluorine substituent at the 2-position and an amino group at the 5-position of the benzene ring, which influences its chemical reactivity and properties. It is typically a white to off-white solid that is soluble in polar solvents like water and alcohols, owing to the presence of the carboxylic acid group. The amino group can participate in hydrogen bonding, enhancing its solubility and reactivity. This compound is of interest in various fields, including pharmaceuticals and materials science, due to its potential applications in drug development and as a building block for synthesizing more complex molecules. Additionally, the presence of the fluorine atom can impart unique electronic properties, making it valuable in medicinal chemistry for modifying biological activity.

Formula: C₇H₆FNO₂

InChI: InChI=1/C7H6FNO2/c8-6-2-1-4(9)3-5(6)7(10)11/h1-3H,9H2,(H,10,11)

SMILES: c1cc(c(cc1N)C(=O)O)F

Synonyms:

• 3-(Difluoromethoxy)-1,1,1,2,2-pentafluoropropane
• Difluoromethyl 2,2,3,3,3-pentafluoropropyl ether
• Propane, 3-(Difluoromethoxy)-1,1,1,2,2-Pentafluoro-
• 5-Amino-2-fluoro-benzoic acid
• 5-Amino-2-fluorobenziocacid
• 5-Amino-2-Fluorobenzioc Acid

5-Amino-2-fluorobenzoic acid

CAS: 56741-33-4

Formula: C₇H₆FNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 155.1264

Ref: IN-DA003MDA

5-Amino-2-fluorobenzoic acid

CAS: 56741-33-4

5-Amino-2-fluorobenzoic acid

Formula: C₇H₆FNO₂

Purity: 97%

Color and Shape: brown to dark brown powder

Molecular weight: 155.13g/mol

Ref: 54-PC1071P

5-Amino-2-fluorobenzoic acid

CAS: 56741-33-4

5-Amino-2-fluorobenzoic acid (5AFBA) is a synthetic aniline that is used as a fluoroquinolone antibiotic. 5AFBA inhibits the synthesis of trehalose, which is vital for bacterial growth. This drug also has been shown to be active against Mycobacterium tuberculosis and Mycobacterium avium complex. 5AFBA has also been shown to have antifungal properties, inhibiting the synthesis of ergosterol in the fungal cell membrane. 5AFBA can be modified by alkylation with geranyl groups or N-methylation at the amino group. These modifications have been shown to increase its antibacterial activity against Pseudomonas aeruginosa.

Formula: C₇H₆FNO₂

Color and Shape: Powder

Molecular weight: 155.13 g/mol

Ref: 3D-FA70089

5-Amino-2-fluorobenzoic acid

CAS: 56741-33-4

Formula: C₇H₆FNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 155.128

Ref: 10-F005488