Description

2,6-Dibromo-3-Methyl-4-Nitroanisole is a halogenated nitroanisole derivative, a key synthetic intermediate in advanced organic chemistry. Its value lies in its unique substitution pattern, which provides specific reactivity for constructing complex molecular architectures. This compound is primarily needed by R&D chemists and process development scientists in the pharmaceutical and agrochemical industries for the synthesis of active ingredients and novel chemical entities.

Application

• Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of active pharmaceutical ingredients (APIs), particularly those requiring brominated aromatic cores.
• Agrochemical Synthesis: Used in the research and production of herbicides, fungicides, and other crop protection agents where its bromine atoms facilitate further functionalization.
• Organic Synthesis & Research: A versatile reagent for coupling reactions (e.g., Suzuki, Buchwald-Hartwig) and as a precursor for more complex heterocyclic compounds in academic and industrial laboratories.
• Dye & Pigment Manufacturing: Acts as an intermediate in the production of specialized dyes and pigments, leveraging the nitro and bromo groups for color and property modification.
• Material Science Research: Investigated as a monomer or precursor for functional polymers and advanced organic materials with specific electronic or optical properties.

Basic Information

Product Name	2,6-Dibromo-3-Methyl-4-Nitroanisole
CAS No.	62265-99-0
Molecular Formula	C8H7Br2NO3
Molecular Weight	324.96 g/mol
Synonyms	1,3-Dibromo-2-methoxy-6-methyl-5-nitrobenzene; 3-Methyl-2,6-dibromo-4-nitroanisole; 2,6-Dibromo-3-methyl-4-nitro-1-methoxybenzene; 5-Nitro-2,6-dibromo-3-methylanisole; Benzene, 1,3-dibromo-2-methoxy-6-methyl-5-nitro-; 2-Methoxy-3-methyl-4,6-dibromonitrobenzene
EINECS	Contact for details

Quality Control

Our 2,6-Dibromo-3-Methyl-4-Nitroanisole is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets exacting standards for research and process chemistry. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and impurity profiles is provided with every shipment and is available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at room temperature (15-25°C). Keep away from heat, sparks, and open flame. Due to its light-sensitive nature, containers should be amber-colored or stored in light-resistant secondary packaging.

Specification

Item	Specification
Appearance	Off-white to light yellow crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 97.0%
Melting Point	Contact for details
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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