Description

Furofenac CAS NO 56983-13-2 is a high-purity pharmaceutical intermediate and chemical building block. This compound is valued for its specific molecular structure, which serves as a critical precursor in the synthesis of advanced active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions and manufacturers in the pharmaceutical and fine chemical industries for the development and production of novel therapeutic agents.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of proprietary active pharmaceutical ingredients (APIs) and drug candidates.
• Organic Synthesis Research: Used in academic and industrial R&D laboratories for constructing complex heterocyclic compounds and exploring new chemical entities.
• Fine Chemical Production: Serves as a precursor in the manufacture of specialty chemicals, agrochemicals, and other high-value organic compounds.
• Reference Standard: Employed as an analytical standard in quality control laboratories for method development and impurity profiling.

Basic Information

Product Name	Furofenac
CAS No.	56983-13-2
Molecular Formula	C13H9NO3
Molecular Weight	227.22 g/mol
Synonyms	2-[(2-Furanylmethyl)amino]benzoic Acid; N-(2-Furfuryl)anthranilic Acid; Furofenac; 2-[(Furan-2-ylmethyl)amino]benzoic Acid; Benzoic acid, 2-[(2-furanylmethyl)amino]-; Furofenacum; Furofenac (USAN)
EINECS	Contact for details

Quality Control

Our Furofenac is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the high standards required for pharmaceutical R&D and production. Certificates of Analysis (COA) documenting all test results are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
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.