Description

4,6-Dinitro-3-(1H)Indazole Carboxaldehyde is a specialized nitroindazole derivative featuring a reactive carboxaldehyde functional group. This compound serves as a critical high-value chemical intermediate for the synthesis of complex heterocyclic molecules. It is primarily utilized by pharmaceutical R&D and agrochemical laboratories for developing novel active ingredients.

Application

• Pharmaceutical Intermediate: Key building block for the synthesis of novel drug candidates, particularly in oncology and anti-inflammatory research.
• Agrochemical Synthesis: Used in the development of advanced herbicides and pesticides due to its nitro-heterocyclic structure.
• Material Science Research: Serves as a precursor for creating specialized dyes, pigments, and photoactive materials.
• Organic Synthesis: The reactive aldehyde group makes it a versatile intermediate for constructing complex molecular libraries via condensation and cyclization reactions.
• Biochemical Probe Development: Used in research to create molecular probes for studying enzyme inhibition and biological pathways.

Basic Information

Product Name	4,6-Dinitro-3-(1H)Indazole Carboxaldehyde
CAS No.	885519-57-3
Molecular Formula	C8H4N4O5
Molecular Weight	236.14 g/mol
Synonyms	3-Formyl-4,6-dinitro-1H-indazole; 4,6-Dinitro-1H-indazole-3-carboxaldehyde; 1H-Indazole-3-carboxaldehyde, 4,6-dinitro-; 4,6-Dinitroindazole-3-carbaldehyde; DNIC
EINECS	Contact for details

Quality Control

Our 4,6-Dinitro-3-(1H)Indazole Carboxaldehyde is manufactured under strict quality control protocols to ensure batch-to-batch consistency and high purity. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing purity, identity, and impurity profiles. Our quality system is designed to meet the stringent requirements of research and development applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). Keep away from heat, sparks, and open flame. Due to its light-sensitive nature, handling should be conducted under subdued lighting or using amber glass containers.

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.