Description

Feloprentan is a high-purity, specialized organic compound identified by CAS No. 204267-33-4, serving as a critical intermediate in advanced pharmaceutical synthesis. Its precise molecular structure makes it invaluable for constructing complex active pharmaceutical ingredients (APIs) with high selectivity and yield. This compound is primarily sought by research institutions and manufacturers in the pharmaceutical and fine chemical industries for developing next-generation therapeutic agents.

Application

Feloprentan (CAS 204267-33-4) is a versatile building block with significant utility in several high-value industrial and research sectors.

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel drug candidates, particularly in central nervous system (CNS) and cardiovascular research.
• Organic Synthesis Research: Used in academic and industrial R&D for constructing complex heterocyclic compounds and exploring new reaction pathways.
• Agrochemical Development: Serves as an intermediate in the research and production of advanced, targeted crop protection agents.
• Material Science: Investigated for its potential in creating specialized polymers and organic electronic materials.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects requiring high-purity intermediates.

Basic Information

Product Name	Feloprentan
CAS No.	204267-33-4
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Feloprentan; 204267-33-4; 1,3-Dihydro-2H-indol-2-one, 1-[(4-fluorophenyl)methyl]-5-(1H-1,2,4-triazol-1-ylmethyl)-; 1-Benzyl-5-(1H-1,2,4-triazol-1-ylmethyl)indolin-2-one; UNII-7VJ28056I4; 7VJ28056I4; BCP31833; SR-01000915113; AKOS025310584; FT-0775785; NS00075813; 1-[(4-Fluorophenyl)methyl]-5-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dihydro-2H-indol-2-one
EINECS	Contact for details

Quality Control

Our Feloprentan is manufactured under strict quality management systems to ensure batch-to-batch consistency and reliability. Each lot undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods. A Certificate of Analysis (COA) detailing all specifications is provided with every shipment, ensuring full traceability and compliance with cGMP guidelines where applicable for pharmaceutical use.

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 the container tightly sealed to protect the light-sensitive material from degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
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.