Cas no 1940-27-8 (4-Bromo-2,5-dichloroaniline)

4-Bromo-2,5-dichloroaniline is a halogenated aniline derivative widely used as an intermediate in organic synthesis, particularly in the production of agrochemicals, pharmaceuticals, and dyes. Its distinct substitution pattern—bromo and chloro groups at the 4, 2, and 5 positions—enhances its reactivity in electrophilic aromatic substitution and coupling reactions, making it valuable for constructing complex molecular frameworks. The compound exhibits high purity and stability under standard conditions, ensuring consistent performance in synthetic applications. Its versatility as a building block for heterocyclic compounds and functionalized aromatic systems underscores its importance in industrial and research settings. Proper handling is advised due to potential toxicity.
4-Bromo-2,5-dichloroaniline structure
4-Bromo-2,5-dichloroaniline structure
Product Name:4-Bromo-2,5-dichloroaniline
CAS No:1940-27-8
MF:C6H4BrCl2N
MW:240.912658691406
MDL:MFCD08444535
CID:232585
PubChem ID:261789
Update Time:2025-10-05

4-Bromo-2,5-dichloroaniline Chemical and Physical Properties

Names and Identifiers

    • Benzenamine,4-bromo-2,5-dichloro-
    • 4-Bromo-2,5-dichloroaniline
    • 4-bromo-2,5-dichlorobenzenamine
    • 2,5-dichloro-4-bromo-aniline
    • 2.5-Dichlor-4-brom-anilin
    • 4-Brom-2,5-dichlor-anilin
    • 4-bromo-2,5-dichloro-aniline
    • 4-bromo-2,5-dichloro-benzenamine
    • Phenol,4-bromo-2,5-dichloro
    • AKOS015855650
    • FT-0692417
    • EN300-65647
    • O11169
    • BAA94027
    • DTXSID60294145
    • MFCD08444535
    • NSC-94731
    • SY073900
    • DS-9991
    • SCHEMBL9629823
    • (4-bromo-2,5-dichlorophenyl)amine
    • 1940-27-8
    • CS-0157847
    • NSC94731
    • STL377203
    • DB-006684
    • MDL: MFCD08444535
    • Inchi: 1S/C6H4BrCl2N/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,10H2
    • InChI Key: SPXFVZDKSRPFPW-UHFFFAOYSA-N
    • SMILES: BrC1=CC(=C(C=C1Cl)N)Cl

Computed Properties

  • Exact Mass: 238.89000
  • Monoisotopic Mass: 238.89042g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 122
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 3.8
  • Topological Polar Surface Area: 26?2

Experimental Properties

  • Density: 1.827±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 91-92 oC
  • Boiling Point: 285.6±35.0 oC (760 Torr),
  • Flash Point: 126.5±25.9 oC,
  • Solubility: Almost insoluble (0.039 g/l) (25 o C),
  • PSA: 26.02000
  • LogP: 3.91930

4-Bromo-2,5-dichloroaniline Customs Data

  • HS CODE:2921420090
  • Customs Data:

    China Customs Code:

    2921420090

    Overview:

    2921420090 Other aniline derivatives and their salts. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

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4-Bromo-2,5-dichloroaniline Production Method

4-Bromo-2,5-dichloroaniline Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:1940-27-8)4-Bromo-2,5-dichloroaniline
Order Number:A1144213
Stock Status:in Stock
Quantity:100g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 22:59
Price ($):268.0

Additional information on 4-Bromo-2,5-dichloroaniline

Comprehensive Analysis of 4-Bromo-2,5-dichloroaniline (CAS No. 1940-27-8): Properties, Applications, and Industry Trends

4-Bromo-2,5-dichloroaniline (CAS No. 1940-27-8) is a halogenated aromatic amine compound with significant relevance in modern chemical research and industrial applications. This brominated dichloroaniline derivative exhibits unique physicochemical properties, making it a valuable intermediate in synthetic chemistry. With the growing demand for specialized organic compounds in pharmaceuticals, agrochemicals, and material science, understanding this chemical's characteristics has become increasingly important for researchers and manufacturers alike.

The molecular structure of 4-Bromo-2,5-dichloroaniline features a benzene ring substituted with bromine at the 4-position and chlorine atoms at the 2- and 5-positions, along with an amino group. This specific arrangement contributes to its electronic properties and reactivity patterns, which are frequently explored in cross-coupling reactions and other transformative processes. Recent studies in green chemistry have investigated more sustainable synthesis routes for such halogenated anilines, addressing environmental concerns while maintaining high yields.

In pharmaceutical applications, 4-Bromo-2,5-dichloroaniline serves as a crucial building block for various active pharmaceutical ingredients (APIs). Its structural features allow for the development of compounds with potential biological activity, particularly in antimicrobial and anti-inflammatory agents. The compound's halogen substituents enhance its ability to participate in diverse chemical transformations, making it valuable for structure-activity relationship studies in drug discovery programs.

The agrochemical industry utilizes 4-Bromo-2,5-dichloroaniline in the synthesis of crop protection agents. Its molecular framework contributes to the development of novel pesticides and herbicides with improved efficacy and environmental profiles. Recent trends in precision agriculture have increased demand for specialized intermediates that can help create targeted solutions for pest management while reducing ecological impact.

Material science applications of 4-Bromo-2,5-dichloroaniline include its use in the production of advanced polymers and dyes. The compound's ability to modify electronic properties makes it interesting for developing functional materials with specific optical or conductive characteristics. Researchers are particularly interested in its potential for creating organic electronic components and photovoltaic materials as part of renewable energy solutions.

Analytical characterization of 4-Bromo-2,5-dichloroaniline typically involves techniques such as HPLC analysis, mass spectrometry, and NMR spectroscopy. These methods ensure purity assessment and structural confirmation, which are critical for research and industrial applications. Recent advancements in analytical chemistry have improved detection limits and accuracy for halogenated aromatic compounds like this one.

Storage and handling recommendations for 4-Bromo-2,5-dichloroaniline emphasize proper containment to maintain stability. The compound should be protected from light and moisture, with optimal storage conditions typically including cool, dry environments. Industry best practices for chemical storage and laboratory safety should always be followed when working with this material.

Market trends indicate steady demand for 4-Bromo-2,5-dichloroaniline, particularly from the pharmaceutical and agrochemical sectors. The global push for specialty chemicals and fine chemical intermediates has created opportunities for manufacturers to develop improved synthesis methods and purification techniques. Recent supply chain challenges have also highlighted the importance of reliable sourcing for such key intermediates.

Environmental considerations surrounding 4-Bromo-2,5-dichloroaniline focus on responsible manufacturing practices and waste management. The chemical industry's shift toward green chemistry principles has led to research into more sustainable production methods for halogenated compounds. Life cycle assessment studies help evaluate the environmental impact of such substances throughout their production and use phases.

Future research directions for 4-Bromo-2,5-dichloroaniline may explore its potential in emerging fields such as bioconjugation chemistry and click chemistry applications. The compound's reactive sites offer possibilities for creating complex molecular architectures with precise functionality. Additionally, computational chemistry approaches are being employed to predict and optimize its reactivity patterns in various synthetic contexts.

Quality control standards for 4-Bromo-2,5-dichloroaniline continue to evolve, with increasing emphasis on analytical method validation and specification compliance. Regulatory requirements in different markets influence the purity standards and documentation needed for commercial distribution. Manufacturers must stay informed about changing regulations to ensure compliance in all target markets.

In conclusion, 4-Bromo-2,5-dichloroaniline (CAS No. 1940-27-8) represents an important chemical intermediate with diverse applications across multiple industries. Its unique structural features and reactivity profile make it valuable for researchers and manufacturers developing innovative solutions in pharmaceuticals, agrochemicals, and advanced materials. As scientific understanding and technological capabilities advance, the potential applications and optimized production methods for this compound will likely continue to expand.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:1940-27-8)4-Bromo-2,5-dichloroaniline
A1144213
Purity:99%
Quantity:100g
Price ($):268.0
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