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2-Amino-5-fluoro-3-(trifluoromethyl)benzoic acid

CAS 1343888-01-6Formula C8H5F4NO2MW 223.12PubChem 63179894

A fluorinated aminobenzoic acid derivative, 2-Amino-5-fluoro-3-(trifluoromethyl)benzoic acid (CAS 1343888-01-6) is primarily utilized as a building block in organic synthesis for research purposes. Its trifluoromethyl and fluoro substituents, along with amino and carboxylic acid groups, make it a versatile intermediate for introducing specific functionalities into target molecules.

Loading RDKit molecule structure...
InChIKey: AQCYKSDNVGASNT-UHFFFAOYSA-NC8H5F4NO2 | MW 223.12

Chemical Identity

Molecular Formula

C8H5F4NO2

Molecular Weight

223.12 g/mol

Exact Mass

223.025641

PubChem CID

63179894

SMILES String

Nc1c(C(=O)O)cc(F)cc1C(F)(F)F

External Identifiers
AKOS012481826AT46691

Catalog Overview

2-Amino-5-fluoro-3-(trifluoromethyl)benzoic acid, identified by CAS 1343888-01-6, is an organic compound featuring a benzoic acid core substituted with an amino group, a fluorine atom, and a trifluoromethyl group. This unique combination of functional groups renders it a valuable chemical intermediate in the synthesis of complex organic molecules. Researchers in medicinal chemistry, agrochemistry, and materials science may find this compound useful for constructing novel scaffolds or modifying existing structures. Its reactivity stems from the amino and carboxylic acid functionalities, while the fluorine and trifluoromethyl groups...

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Read more catalog context

2-Amino-5-fluoro-3-(trifluoromethyl)benzoic acid, identified by CAS 1343888-01-6, is an organic compound featuring a benzoic acid core substituted with an amino group, a fluorine atom, and a trifluoromethyl group. This unique combination of functional groups renders it a valuable chemical intermediate in the synthesis of complex organic molecules. Researchers in medicinal chemistry, agrochemistry, and materials science may find this compound useful for constructing novel scaffolds or modifying existing structures. Its reactivity stems from the amino and carboxylic acid functionalities, while the fluorine and trifluoromethyl groups can impart specific electronic and steric properties to synthesized compounds, influencing their biological activity or material characteristics. This compound is intended for Research Use Only (RUO).

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline powder

Physical State

Solid

Melting Point

200.0 °C

Boiling Point

350.0 °C

Density

1.5 g/cm³

Water Solubility

Slightly soluble

Flash Point

205.0 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle 2-Amino-5-fluoro-3-(trifluoromethyl)benzoic acid in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety goggles, gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for comprehensive safety information before use. This compound is for Research Use Only.

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