Description

5-Benzyltetrahydro-3Ah-Furo[3,4-C]Pyrrole-1,3-Dione is a high-purity, advanced pharmaceutical intermediate with a complex heterocyclic structure. This compound is critical for the synthesis of novel active pharmaceutical ingredients (APIs) and serves as a key building block in modern medicinal chemistry. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of new therapeutic agents, particularly within the fields of central nervous system (CNS) and metabolic disorder research.

Application

• Pharmaceutical Intermediate: A crucial precursor in the multi-step synthesis of proprietary drug candidates and novel chemical entities.
• Medicinal Chemistry Research: Used as a versatile scaffold for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• API Development: Serves as a key building block for the production of complex, high-value active pharmaceutical ingredients.
• Contract Research & Manufacturing (CRO/CMO): Supplied to organizations specializing in custom synthesis and process development for the pharmaceutical industry.
• Academic Research: Employed in university and institutional labs for investigating new synthetic methodologies and heterocyclic chemistry.

Basic Information

Product Name	5-Benzyltetrahydro-3Ah-Furo[3,4-C]Pyrrole-1,3-Dione
CAS No.	1221289-17-3
Molecular Formula	C15H15NO3
Molecular Weight	257.29 g/mol
Synonyms	5-Benzyltetrahydro-3aH-furo[3,4-c]pyrrole-1,3-dione; 5-Benzyl-1,2,3,3a-tetrahydro-4H-furo[3,4-c]pyrrole-1,3-dione; 5-Benzyl-3a,4,5,6-tetrahydro-3H-furo[3,4-c]pyrrole-1,3-dione; 5-Benzyl-3a,4,5,6-tetrahydrofuro[3,4-c]pyrrole-1,3-dione; 1221289-17-3; Furo[3,4-c]pyrrole-1,3-dione, 5-benzyltetrahydro-3aH-
EINECS	Contact for details

Quality Control

Our 5-Benzyltetrahydro-3Ah-Furo[3,4-C]Pyrrole-1,3-Dione is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with every shipment, detailing all specifications and test results. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical research and development processes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame. For long-term storage, consider storing under an inert atmosphere to maintain optimal stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (NMR)	Conforms to structure
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5% Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 0.5%
Heavy Metals	≤ 20 ppm

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