Description

5-(3-Chloro-4-Fluoro-Phenoxymethyl)-Furan-2-Carboxylic Acid is a high-purity, advanced pharmaceutical intermediate characterized by its specific halogenated phenoxymethyl furan structure. This compound is critical for the synthesis of novel active pharmaceutical ingredients (APIs), particularly in therapeutic areas requiring precise molecular frameworks. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new chemical entities and complex organic molecules. The material is supplied with a focus on batch-to-batch consistency and reliable purity to support stringent R&D and scale-up processes.

Application

• Pharmaceutical Intermediate: Key building block in the synthesis of novel drug candidates and active pharmaceutical ingredients (APIs).
• Agrochemical Research: Used in the development of new herbicides and pesticides due to its halogenated aromatic structure.
• Material Science: Serves as a monomer or precursor for specialized polymers and advanced organic materials.
• Chemical Synthesis: A versatile reagent for constructing complex heterocyclic and aryl ether compounds in organic chemistry.
• Life Science Research: Employed in biochemical and pharmacological studies as a reference standard or probe molecule.

Basic Information

Product Name	5-(3-Chloro-4-Fluoro-Phenoxymethyl)-Furan-2-Carboxylic Acid
CAS No.	832737-77-6
Molecular Formula	C12H8ClFO4
Molecular Weight	270.64 g/mol
Synonyms	5-[(3-Chloro-4-fluorophenoxy)methyl]-2-furancarboxylic acid; 2-Furancarboxylic acid, 5-[(3-chloro-4-fluorophenoxy)methyl]-; 5-((3-Chloro-4-fluorophenoxy)methyl)furan-2-carboxylic acid; 3-Chloro-4-fluoro-5-(furan-2-carboxymethyl)phenol derivative; 832737-77-6; Halogenated furan carboxylic acid intermediate; Phenoxymethyl furan carboxylate
EINECS	Contact for details

Quality Control

Our production of 5-(3-Chloro-4-Fluoro-Phenoxymethyl)-Furan-2-Carboxylic Acid adheres to a strict quality management system to ensure product integrity and traceability. Each batch is analyzed using advanced analytical techniques, including HPLC, GC, and NMR, to verify identity, purity, and the absence of specified impurities. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment. We support compliance with cGMP and ISO standards for pharmaceutical intermediates, and custom purity grades are available to meet specific project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from heat, open flames, and incompatible materials. The container should be kept tightly sealed when not in use to protect against moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Any single unknown impurity	≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.