Description

.Trans.-1,3-Dibenzyl-Dihydro-1H-Furo[3,4-D]Imidazole-2,4,6(3H)-Trione is a specialized heterocyclic organic compound featuring a fused furoimidazole trione core structure with benzyl substituents. This compound is valued for its role as a key synthetic intermediate and building block in advanced organic synthesis, particularly for constructing complex nitrogen- and oxygen-containing heterocycles. It is primarily utilized by research institutions and industrial R&D departments in the pharmaceutical and agrochemical sectors for the development of novel active ingredients.

Application

• Pharmaceutical Intermediate: Serves as a crucial precursor in the synthesis of potential drug candidates, especially those targeting neurological or metabolic pathways.
• Agrochemical Research: Used as a building block for developing new herbicides, fungicides, or insecticides with novel modes of action.
• Organic Synthesis Reagent: Acts as a versatile scaffold for constructing complex heterocyclic libraries in medicinal and combinatorial chemistry.
• Material Science Research: Investigated as a monomer or precursor for specialty polymers and advanced organic materials.
• Academic & R&D Laboratories: Employed in fundamental chemical research to study reaction mechanisms and develop new synthetic methodologies.

Basic Information

Product Name	.Trans.-1,3-Dibenzyl-Dihydro-1H-Furo[3,4-D]Imidazole-2,4,6(3H)-Trione
CAS No.	26340-00-1
Molecular Formula	C20H16N2O4
Molecular Weight	348.35 g/mol
Synonyms	1,3-Dibenzyltetrahydro-1H-furo[3,4-d]imidazole-2,4,6(3H)-trione; trans-1,3-Dibenzyl-1,3,3a,6a-tetrahydro-1H-furo[3,4-d]imidazole-2,4,6-trione; 1H-Furo[3,4-d]imidazole-2,4,6(3H)-trione, dihydro-1,3-dibenzyl-, (3aR,6aS)-rel-; Furo[3,4-d]imidazole-2,4,6-trione derivative; DBFIT; Contact for additional synonyms.
EINECS	Contact for details

Quality Control

Our .Trans.-1,3-Dibenzyl-Dihydro-1H-Furo[3,4-D]Imidazole-2,4,6(3H)-Trione is produced under strict quality management protocols. Each batch undergoes comprehensive analytical testing, including chromatographic purity assays and structural confirmation, to ensure high consistency and reliability for research and development applications. Certificates of Analysis (COA) detailing specific batch results are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to minimize exposure to atmospheric humidity.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Melting Point	Contact for details
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%

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