Cas no 80026-20-6 (BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO-)

1-Bromo-3-chloro-2-methyl-4-nitrobenzene is a halogenated aromatic compound with a molecular formula of C7H5BrClNO2. It features a benzene ring substituted with bromine at the 1-position, chlorine at the 3-position, a methyl group at the 2-position, and a nitro group at the 4-position. This structure imparts unique reactivity, making it valuable in organic synthesis, particularly in electrophilic aromatic substitution and nucleophilic displacement reactions. The presence of multiple functional groups allows for selective modifications, enabling its use as an intermediate in pharmaceuticals, agrochemicals, and specialty chemicals. Its crystalline solid form ensures stability and ease of handling under standard conditions. The compound's well-defined substitution pattern enhances its utility in regioselective synthesis.
BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- structure
80026-20-6 structure
Product Name:BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO-
CAS No:80026-20-6
MF:C7H5BrClNO2
MW:250.477100133896
CID:3373257
Update Time:2026-04-24

BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- Chemical and Physical Properties

Names and Identifiers

    • BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO-

BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- Pricemore >>

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Additional information on BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO-

Comprehensive Overview of BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- (CAS No. 80026-20-6)

BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- (CAS No. 80026-20-6) is a specialized aromatic compound widely utilized in organic synthesis and industrial applications. This compound features a benzene ring substituted with bromo, chloro, methyl, and nitro functional groups, making it a versatile intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. The unique combination of substituents enhances its reactivity, enabling precise modifications in synthetic pathways.

In recent years, the demand for nitro-substituted benzene derivatives has surged due to their role in developing high-performance materials and active pharmaceutical ingredients (APIs). Researchers and manufacturers are particularly interested in 1-Bromo-3-chloro-2-methyl-4-nitrobenzene for its potential in green chemistry applications, where efficiency and sustainability are prioritized. The compound’s structural properties align with modern trends in atom-economical synthesis and catalysis, addressing key challenges in chemical manufacturing.

The synthesis of BENZENE, 1-BROMO-3-CHLORO-2-METHYL-4-NITRO- involves multi-step reactions, including halogenation and nitration processes. Advanced analytical techniques such as NMR spectroscopy and HPLC are employed to ensure high purity and consistency, meeting stringent industry standards. Its stability under controlled conditions makes it suitable for storage and transportation, though proper handling protocols must be followed to maintain integrity.

From an environmental perspective, the compound’s degradation pathways and ecotoxicological profile are subjects of ongoing research. Innovations in biodegradable solvents and waste reduction strategies are being explored to minimize its ecological footprint. These efforts resonate with global initiatives like the UN Sustainable Development Goals (SDGs), particularly in responsible consumption and production.

In the pharmaceutical sector, 80026-20-6 serves as a precursor for antimicrobial and anti-inflammatory agents. Its nitro group is pivotal in drug design, enabling interactions with biological targets. Recent studies highlight its utility in cancer research, where modified benzene derivatives exhibit promising activity against tumor cells. Such applications underscore the compound’s relevance in addressing contemporary health challenges.

Industrial users frequently search for suppliers of 1-Bromo-3-chloro-2-methyl-4-nitrobenzene or inquire about technical specifications and safety data sheets (SDS). Additionally, queries about scalability and cost-effective synthesis routes reflect market priorities. Addressing these concerns, manufacturers are adopting continuous flow chemistry to enhance yield and reduce production costs.

Looking ahead, the compound’s adaptability positions it as a key player in emerging fields like nanotechnology and smart materials. Its integration into electronic coatings and photovoltaic devices demonstrates cross-industry potential. Collaborative R&D efforts are expected to unlock further innovations, reinforcing its significance in science and technology.

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