Description

1H-Benzimidazole, 6-Nitro-2-Phenyl- is a specialized heterocyclic organic compound featuring a benzimidazole core structure substituted with nitro and phenyl groups. This molecular architecture makes it a valuable intermediate for synthesizing more complex molecules with targeted biological or material properties. It is primarily sought by research and development teams in the pharmaceutical and agrochemical sectors for creating novel active ingredients.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the research and synthesis of potential drug candidates, particularly those targeting specific enzyme pathways.
• Agrochemical Research: Used in developing new herbicides, fungicides, or pesticides, leveraging its heterocyclic structure for bioactivity.
• Dye and Pigment Synthesis: Acts as a precursor for creating specialized dyes, pigments, or optical brighteners due to the presence of the nitro and aromatic groups.
• Material Science: Investigated for use in organic electronics, such as in the development of organic light-emitting diodes (OLEDs) or charge-transport materials.
• Coordination Chemistry: Functions as a ligand for metal complexes in catalytic or sensor applications, utilizing the nitrogen atoms in the benzimidazole ring.
• Academic & Industrial R&D: Employed in chemical research for method development, structure-activity relationship (SAR) studies, and exploring new chemical entities.

Basic Information

Product Name	1H-Benzimidazole, 6-Nitro-2-Phenyl-
CAS No.	1571-85-3
Molecular Formula	C₁₃H₉N₃O₂
Molecular Weight	239.23 g/mol
Synonyms	6-Nitro-2-phenyl-1H-benzimidazole; 2-Phenyl-6-nitrobenzimidazole; 6-Nitro-2-phenylbenzimidazole; NSC 403697; Benzimidazole, 6-nitro-2-phenyl-; 1H-Benzimidazole, 6-nitro-2-phenyl-; 6-Nitro-2-phenyl-1H-benzo[d]imidazole
EINECS	Contact for details

Quality Control

Our 1H-Benzimidazole, 6-Nitro-2-Phenyl- is produced under strict quality management protocols. 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 research and industrial synthesis. Certificates of Analysis (COA) with detailed batch-specific results are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at room temperature (15-25°C). Keep away from heat sources and incompatible materials.

Specification

Item	Specification
Appearance	Yellow to orange crystalline powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Melting Point	Contact for details
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.