Cas no 296246-80-5 (2-(2-Amino-4,6-dinitro-phenyl)-ethanol)

2-(2-Amino-4,6-dinitro-phenyl)-ethanol is a nitroaromatic compound featuring both amino and hydroxyl functional groups, making it a versatile intermediate in organic synthesis. Its structure allows for selective reactivity in electrophilic and nucleophilic substitutions, facilitating applications in dye, pharmaceutical, and agrochemical production. The presence of electron-withdrawing nitro groups enhances its stability while enabling further functionalization. The compound's balanced solubility in polar and organic solvents improves its utility in diverse reaction conditions. Careful handling is required due to its nitroaromatic properties, but its well-defined reactivity profile makes it a valuable building block for complex molecular architectures.
2-(2-Amino-4,6-dinitro-phenyl)-ethanol structure
296246-80-5 structure
Product Name:2-(2-Amino-4,6-dinitro-phenyl)-ethanol
CAS No:296246-80-5
MF:C8H9N3O5
MW:227.174161672592
CID:3103004
PubChem ID:4395373
Update Time:2025-10-05

2-(2-Amino-4,6-dinitro-phenyl)-ethanol Chemical and Physical Properties

Names and Identifiers

    • 2-(2-Amino-4,6-dinitro-phenyl)-ethanol
    • AKOS001736445
    • SR-01000090124
    • 296246-80-5
    • SR-01000090124-1
    • STK758443
    • 2-(2-amino-4,6-dinitrophenyl)ethanol
    • 2-(2-amino-4,6-dinitrophenyl)ethan-1-ol
    • Inchi: 1S/C8H9N3O5/c9-7-3-5(10(13)14)4-8(11(15)16)6(7)1-2-12/h3-4,12H,1-2,9H2
    • InChI Key: WOQFNZMZQCITII-UHFFFAOYSA-N
    • SMILES: OCCC1C(=CC(=CC=1[N+](=O)[O-])[N+](=O)[O-])N

Computed Properties

  • Exact Mass: 227.05422040Da
  • Monoisotopic Mass: 227.05422040Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 2
  • Complexity: 274
  • 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: 0.5
  • Topological Polar Surface Area: 138?2

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Additional information on 2-(2-Amino-4,6-dinitro-phenyl)-ethanol

Comprehensive Analysis of 2-(2-Amino-4,6-dinitro-phenyl)-ethanol (CAS No. 296246-80-5)

2-(2-Amino-4,6-dinitro-phenyl)-ethanol (CAS No. 296246-80-5) is a specialized organic compound that has garnered significant attention in recent years due to its unique chemical structure and potential applications in various industries. This compound, characterized by its nitro and amino functional groups, is often studied for its reactivity and utility in synthetic chemistry. Researchers and industry professionals frequently search for terms like "2-(2-Amino-4,6-dinitro-phenyl)-ethanol synthesis" or "CAS 296246-80-5 properties," highlighting the growing interest in this molecule.

The molecular structure of 2-(2-Amino-4,6-dinitro-phenyl)-ethanol features a benzene ring substituted with two nitro groups at the 4 and 6 positions, an amino group at the 2 position, and an ethanol side chain. This arrangement imparts distinct chemical properties, making it a subject of interest in fields such as pharmaceuticals, agrochemicals, and materials science. Searches for "nitro-phenyl derivatives applications" or "amino-nitro compounds in drug development" reflect the broader curiosity about its uses.

One of the key reasons for the popularity of 2-(2-Amino-4,6-dinitro-phenyl)-ethanol is its role as an intermediate in organic synthesis. Its nitro groups are highly reactive, enabling transformations into other functional groups like amines or hydroxylamines. This versatility aligns with current trends in green chemistry, where researchers seek efficient and sustainable synthetic routes. Queries such as "eco-friendly nitro compound synthesis" or "CAS 296246-80-5 in green chemistry" underscore this focus.

In the pharmaceutical sector, 2-(2-Amino-4,6-dinitro-phenyl)-ethanol is explored for its potential as a building block in drug design. The presence of both amino and nitro groups allows for the creation of diverse pharmacophores, which are critical in developing new therapeutics. Recent searches like "nitro-phenyl ethanol derivatives in medicine" or "CAS 296246-80-5 biological activity" indicate a strong interest in its biomedical applications.

From an industrial perspective, this compound is also relevant in the development of advanced materials. Its aromatic core and functional groups make it a candidate for creating polymers or coatings with specific properties. Terms such as "high-performance materials from nitro compounds" or "2-(2-Amino-4,6-dinitro-phenyl)-ethanol in material science" are increasingly common in academic and industrial discussions.

Safety and handling of 2-(2-Amino-4,6-dinitro-phenyl)-ethanol are also topics of interest. While it is not classified as a hazardous material, proper storage and handling protocols are essential due to its reactive nitro groups. Searches like "safe handling of nitro-phenyl compounds" or "CAS 296246-80-5 storage guidelines" reflect this concern among users.

In conclusion, 2-(2-Amino-4,6-dinitro-phenyl)-ethanol (CAS No. 296246-80-5) is a multifaceted compound with significant potential across multiple disciplines. Its unique structure and reactivity make it a valuable subject for ongoing research, particularly in synthetic chemistry, pharmaceuticals, and materials science. The frequent searches for related keywords demonstrate its relevance in contemporary scientific and industrial landscapes.

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