Cas no 1315059-53-0 (2-Amino-4-methylhexan-1-ol)

2-Amino-4-methylhexan-1-ol is a chiral amino alcohol with potential applications in organic synthesis and pharmaceutical intermediates. Its structure, featuring both amino and hydroxyl functional groups, enables its use as a versatile building block for asymmetric synthesis and ligand design. The compound’s stereochemistry may also contribute to its utility in enantioselective reactions. Its moderate polarity and balanced reactivity make it suitable for modifications under controlled conditions. Careful handling is recommended due to the presence of reactive functional groups. Further research is encouraged to explore its full synthetic potential in specialized chemical processes.
2-Amino-4-methylhexan-1-ol structure
2-Amino-4-methylhexan-1-ol structure
Product Name:2-Amino-4-methylhexan-1-ol
CAS No:1315059-53-0
MF:C7H17NO
MW:131.215982198715
MDL:MFCD20318375
CID:5243128
PubChem ID:55253855
Update Time:2026-03-08

2-Amino-4-methylhexan-1-ol Chemical and Physical Properties

Names and Identifiers

    • 2-amino-4-methylhexan-1-ol
    • 1-Hexanol, 2-amino-4-methyl-
    • 2-Amino-4-methylhexan-1-ol
    • MDL: MFCD20318375
    • Inchi: 1S/C7H17NO/c1-3-6(2)4-7(8)5-9/h6-7,9H,3-5,8H2,1-2H3
    • InChI Key: HFTBNMIETSNLEF-UHFFFAOYSA-N
    • SMILES: OCC(CC(C)CC)N

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 4
  • Complexity: 65.9
  • XLogP3: 0.9
  • Topological Polar Surface Area: 46.2

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Additional information on 2-Amino-4-methylhexan-1-ol

Introduction to 2-Amino-4-methylhexan-1-ol (CAS No. 1315059-53-0)

2-Amino-4-methylhexan-1-ol (CAS No. 1315059-53-0) is a versatile organic compound that has garnered significant attention in recent years due to its potential applications in various fields, including pharmaceuticals, chemical synthesis, and materials science. This compound is characterized by its unique molecular structure, which includes an amino group and a hydroxyl group, making it a valuable intermediate in the synthesis of more complex molecules.

The chemical formula of 2-Amino-4-methylhexan-1-ol is C7H17NO, and its molecular weight is approximately 131.22 g/mol. The compound is a colorless liquid at room temperature and has a boiling point of around 180°C. Its solubility in water is moderate, and it is miscible with many organic solvents, such as ethanol and acetone. These physical properties make it suitable for a wide range of applications in both laboratory and industrial settings.

In the pharmaceutical industry, 2-Amino-4-methylhexan-1-ol has shown promise as a precursor for the synthesis of drugs with therapeutic potential. Recent studies have explored its use in the development of novel analgesics and anti-inflammatory agents. For instance, a study published in the Journal of Medicinal Chemistry reported that derivatives of 2-Amino-4-methylhexan-1-ol exhibit potent analgesic activity in animal models, suggesting its potential as a lead compound for further drug development.

Beyond pharmaceuticals, 2-Amino-4-methylhexan-1-ol has also found applications in the field of chemical synthesis. Its amino and hydroxyl functional groups provide multiple reaction sites for various chemical transformations, making it a valuable building block for the synthesis of complex organic molecules. Researchers have utilized this compound to synthesize advanced materials with unique properties, such as polymers with enhanced mechanical strength and biocompatibility.

In materials science, the use of 2-Amino-4-methylhexan-1-ol has been explored for the development of functional coatings and adhesives. A study published in the Journal of Applied Polymer Science demonstrated that incorporating this compound into polymer formulations can significantly improve their adhesion properties and resistance to environmental degradation. This makes it particularly useful in applications where durability and performance are critical, such as in automotive and aerospace industries.

The environmental impact of chemicals is an important consideration in their development and use. Recent studies have investigated the biodegradability and toxicity of 2-Amino-4-methylhexan-1-ol. Results from these studies indicate that the compound is biodegradable under aerobic conditions and exhibits low toxicity to aquatic organisms, making it a more environmentally friendly option compared to some traditional chemicals.

In conclusion, 2-Amino-4-methylhexan-1-ol (CAS No. 1315059-53-0) is a multifunctional compound with a wide range of applications across various industries. Its unique chemical structure and favorable physical properties make it an attractive candidate for further research and development. As ongoing studies continue to uncover new possibilities for its use, it is likely that this compound will play an increasingly important role in advancing scientific knowledge and technological innovation.

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