Cas no 1199-47-9 (2-Amino-5-tert-butylphenol)

2-Amino-5-tert-butylphenol is a substituted phenolic compound featuring both an amino group and a tert-butyl group on the aromatic ring. This structural configuration imparts unique reactivity, making it a valuable intermediate in organic synthesis, particularly for the preparation of dyes, pharmaceuticals, and specialty chemicals. The tert-butyl group enhances steric hindrance, influencing selectivity in coupling reactions, while the amino group provides a versatile site for further functionalization. Its stability under various conditions and compatibility with multiple reaction pathways make it a practical choice for researchers. The compound is typically handled under standard laboratory precautions due to its potential sensitivity to oxidation and light.
2-Amino-5-tert-butylphenol structure
2-Amino-5-tert-butylphenol structure
Product Name:2-Amino-5-tert-butylphenol
CAS No:1199-47-9
MF:C10H15NO
MW:165.232202768326
MDL:MFCD16996854
CID:1212287
PubChem ID:15294169
Update Time:2025-06-29

2-Amino-5-tert-butylphenol Chemical and Physical Properties

Names and Identifiers

    • Phenol, 2-amino-5-(1,1-dimethylethyl)-
    • 2-amino-5-tert-butylphenol
    • 1199-47-9
    • BAA19947
    • 2-amino-5-(tert-butyl)phenol
    • D94464
    • HFCOMOKKPQIADM-UHFFFAOYSA-N
    • MFCD16996854
    • SY045107
    • MB21776
    • SCHEMBL1024107
    • STR11871
    • EN300-196875
    • CS-0161453
    • AKOS037655970
    • DTXSID80571081
    • 2-Amino-5-tert-butylphenol
    • MDL: MFCD16996854
    • Inchi: 1S/C10H15NO/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,12H,11H2,1-3H3
    • InChI Key: HFCOMOKKPQIADM-UHFFFAOYSA-N
    • SMILES: OC1=C(C=CC(=C1)C(C)(C)C)N

Computed Properties

  • Exact Mass: 165.115364102g/mol
  • Monoisotopic Mass: 165.115364102g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 1
  • Complexity: 150
  • 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: 2.6
  • Topological Polar Surface Area: 46.2?2

2-Amino-5-tert-butylphenol Pricemore >>

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Additional information on 2-Amino-5-tert-butylphenol

Professional Introduction to 2-Amino-5-tert-butylphenol (CAS No. 1199-47-9)

2-Amino-5-tert-butylphenol, identified by the Chemical Abstracts Service Number (CAS No.) 1199-47-9, is a significant organic compound with a wide range of applications in the chemical and pharmaceutical industries. This compound, characterized by its amino and tert-butyl substituents on a phenolic backbone, exhibits unique chemical properties that make it valuable in various synthetic processes and biological studies.

The molecular structure of 2-Amino-5-tert-butylphenol consists of a benzene ring substituted with an amino group at the 2-position and a tert-butyl group at the 5-position. This arrangement imparts distinct reactivity and stability, making it a versatile intermediate in organic synthesis. The presence of both electron-donating (amino) and electron-withdrawing (tert-butyl) groups allows for diverse functionalization, enabling its use in the development of complex molecules.

In recent years, 2-Amino-5-tert-butylphenol has garnered attention in academic and industrial research due to its potential applications in pharmaceuticals. Studies have highlighted its role as a precursor in the synthesis of bioactive molecules, including intermediates for drug candidates targeting various therapeutic areas. The compound's ability to undergo selective modifications makes it particularly useful in medicinal chemistry.

One of the most compelling aspects of 2-Amino-5-tert-butylphenol is its utility in the development of novel antimicrobial agents. Research has demonstrated that derivatives of this compound exhibit promising activity against resistant bacterial strains. The tert-butyl group enhances lipophilicity, improving membrane penetration, while the amino group facilitates interactions with biological targets. These properties are critical in designing effective antimicrobial therapies.

Additionally, 2-Amino-5-tert-butylphenol has been explored in the context of antioxidant and anti-inflammatory applications. Its phenolic structure contributes to radical scavenging capabilities, making it a candidate for formulations aimed at reducing oxidative stress. Preliminary studies suggest that certain derivatives may modulate inflammatory pathways, offering potential benefits in chronic disease management.

The synthesis of 2-Amino-5-tert-butylphenol typically involves aromatic substitution reactions, where appropriate precursors are selected based on yield and purity requirements. Advances in catalytic methods have improved the efficiency of these processes, reducing waste and energy consumption. Such innovations align with growing demands for sustainable chemical manufacturing practices.

In industrial settings, 2-Amino-5-tert-butylphenol is valued for its role in producing specialty chemicals used in coatings, adhesives, and polymers. Its structural features contribute to material properties such as thermal stability and mechanical strength. By integrating this compound into formulations, manufacturers can enhance product performance while maintaining cost-effectiveness.

From an environmental perspective, the handling and disposal of 2-Amino-5-tert-butylphenol must adhere to stringent guidelines to ensure safety and minimize ecological impact. Proper storage conditions and waste management protocols are essential to prevent unintended consequences. Regulatory bodies continue to refine standards to address emerging challenges in chemical safety.

The future prospects of 2-Amino-5-tert-butylphenol are promising, with ongoing research expanding its potential applications. Collaborative efforts between academia and industry are driving innovation, particularly in drug discovery and advanced materials science. As our understanding of molecular interactions deepens, so too will the utility of this versatile compound.

In conclusion, 2-Amino-5-tert-butylphenol (CAS No. 1199-47-9) represents a cornerstone in modern chemical research due to its multifaceted roles across pharmaceuticals, materials science, and industrial chemistry. Its unique structural attributes enable diverse applications, while continued advancements promise to unlock new possibilities for this remarkable compound.

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