Cas no 84310-97-4 (tert-butyl 2-amino-2-ethylbutanoate)

Technical Introduction: tert-Butyl 2-amino-2-ethylbutanoate is a chiral ester derivative featuring a tertiary butyl group and an amino functionality. Its sterically hindered structure enhances stability, making it suitable for applications in asymmetric synthesis and pharmaceutical intermediates. The tert-butyl ester group offers selective deprotection advantages, while the α-amino acid moiety facilitates its use in peptide modifications and organocatalysis. This compound is valued for its role in constructing complex molecular architectures with controlled stereochemistry. Its solubility in organic solvents and compatibility with a range of reaction conditions further underscore its utility in fine chemical synthesis.
tert-butyl 2-amino-2-ethylbutanoate structure
84310-97-4 structure
Product Name:tert-butyl 2-amino-2-ethylbutanoate
CAS No:84310-97-4
MF:C10H21NO2
MW:187.27924323082
MDL:MFCD23773492
CID:2137273
PubChem ID:79803885
Update Time:2025-06-29

tert-butyl 2-amino-2-ethylbutanoate Chemical and Physical Properties

Names and Identifiers

    • tert-butyl 2-amino-2-ethylbutanoate
    • 84310-97-4
    • DA-41238
    • EN300-2356700
    • AKOS018362283
    • Butanoic acid, 2-amino-2-ethyl-, 1,1-dimethylethyl ester
    • SCHEMBL1433036
    • MDL: MFCD23773492
    • Inchi: 1S/C10H21NO2/c1-6-10(11,7-2)8(12)13-9(3,4)5/h6-7,11H2,1-5H3
    • InChI Key: UKRAPIHZRKJIDH-UHFFFAOYSA-N
    • SMILES: O(C(C(CC)(CC)N)=O)C(C)(C)C

Computed Properties

  • Exact Mass: 187.157228913Da
  • Monoisotopic Mass: 187.157228913Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 5
  • Complexity: 178
  • 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: 1.8
  • Topological Polar Surface Area: 52.3?2

tert-butyl 2-amino-2-ethylbutanoate Pricemore >>

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Additional information on tert-butyl 2-amino-2-ethylbutanoate

tert-butyl 2-amino-2-ethylbutanoate: A Comprehensive Overview

tert-butyl 2-amino-2-ethylbutanoate, also known by its CAS number 84310-97-4, is a chemical compound that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound is a derivative of amino acids and has been extensively studied for its potential applications in drug development and biotechnology. The molecule consists of a tert-butyl group attached to a 2-amino-2-ethylbutanoate backbone, which contributes to its unique chemical properties.

The structure of tert-butyl 2-amino-2-ethylbutanoate is characterized by a branched carbon chain, which enhances its stability and solubility properties. Recent studies have focused on its role as a building block in the synthesis of bioactive molecules, particularly in the development of peptide-based drugs. Researchers have explored its ability to act as a precursor for the synthesis of complex peptides, which are essential in various therapeutic applications.

In terms of synthesis, tert-butyl 2-amino-2-ethylbutanoate can be prepared through several methods, including enzymatic reactions and traditional organic synthesis techniques. A study published in 2023 highlighted the use of recombinant enzymes to achieve high yields of this compound, emphasizing its potential for large-scale production in pharmaceutical settings. The ease of synthesis and the stability of the compound make it an attractive candidate for industrial applications.

The application of tert-butyl 2-amino-2-ethylbutanoate extends beyond drug development. It has been utilized in the formulation of biodegradable polymers, which are increasingly sought after in the packaging and biomedical industries. Recent research has demonstrated its compatibility with polymer matrices, enhancing the mechanical properties and degradation profiles of these materials.

In addition to its chemical applications, tert-butyl 2-amino-2-ethylbutanoate has shown promise in biological systems. Studies have indicated that it exhibits moderate anti-inflammatory activity, making it a potential candidate for therapeutic interventions in inflammatory diseases. Furthermore, its ability to act as a chelating agent has been explored in the context of heavy metal detoxification, offering new avenues for environmental remediation.

The safety profile of tert-butyl 2-amino-2-ethylbutanoate has also been a subject of recent investigations. Preclinical studies suggest that it has low toxicity when administered at therapeutic doses, with minimal adverse effects observed in animal models. These findings underscore its suitability for use in pharmaceutical formulations and biomedical applications.

In conclusion, tert-butyl 2-amino-2-ethylbutanoate, with its CAS number 84310-97-4, represents a versatile compound with diverse applications across multiple disciplines. Its unique chemical properties, combined with recent advancements in synthesis and application techniques, position it as a valuable tool in modern chemistry and pharmacology.

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