Cas no 60793-95-5 (Diethyl 3-aminopentanedioate)

Diethyl 3-aminopentanedioate is a diester derivative of glutamic acid, featuring both ester and amine functional groups. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its bifunctional reactivity allows for versatile modifications, enabling the formation of amides, esters, or other derivatives through selective reactions. The ester groups enhance solubility in organic solvents, facilitating purification and further transformations. The presence of the amine moiety provides a handle for additional functionalization, making it valuable for constructing complex molecular architectures. Its stability under standard conditions ensures reliable handling and storage.
Diethyl 3-aminopentanedioate structure
Diethyl 3-aminopentanedioate structure
Product Name:Diethyl 3-aminopentanedioate
CAS No:60793-95-5
MF:C9H18ClNO4
MW:239.69652223587
CID:953536
PubChem ID:24190535
Update Time:2025-10-22

Diethyl 3-aminopentanedioate Chemical and Physical Properties

Names and Identifiers

    • Diethyl 3-aminopentanedioate
    • NSC-110353
    • NSC110353
    • diethyl 3-aminopentanedioate;hydrochloride
    • BS-46033
    • Diethyl 3-aminopentanedioate hydrochloride
    • 60793-95-5
    • SCHEMBL3637939
    • 1,5-diethyl 3-aminopentanedioate hydrochloride
    • CS-0161136
    • D81408
    • Inchi: 1S/C9H17NO4.ClH/c1-3-13-8(11)5-7(10)6-9(12)14-4-2;/h7H,3-6,10H2,1-2H3;1H
    • InChI Key: XCTVAGMMVHLHQU-UHFFFAOYSA-N
    • SMILES: Cl.O(CC)C(CC(CC(=O)OCC)N)=O

Computed Properties

  • Exact Mass: 203.11581
  • Monoisotopic Mass: 239.0924357g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 8
  • Complexity: 173
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 78.6?2

Experimental Properties

  • PSA: 78.62

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Additional information on Diethyl 3-aminopentanedioate

Diethyl 3-Aminopentanedioate: A Comprehensive Overview

Diethyl 3-aminopentanedioate (CAS No. 60793-95-5) is a compound of significant interest in the fields of organic chemistry and biochemistry. This compound, also referred to as diethyl amino adipate, is a derivative of 3-aminopentanedioic acid, which is a naturally occurring amino acid. The diethyl ester form of this compound has been studied extensively for its potential applications in various industries, including pharmaceuticals, agriculture, and biotechnology.

The molecular structure of diethyl 3-aminopentanedioate consists of a pentanedioic acid backbone with an amino group at the third carbon position. The two ethyl ester groups attached to the carboxylic acid moieties make this compound highly soluble in organic solvents, which is advantageous for its use in various chemical reactions. Recent studies have highlighted the importance of this compound in the synthesis of biodegradable polymers, which are increasingly being explored as sustainable alternatives to traditional plastics.

One of the most promising applications of diethyl 3-aminopentanedioate lies in its role as a precursor for the production of polyamides and polyesters. These polymers are known for their excellent mechanical properties and biocompatibility, making them ideal for use in medical devices and tissue engineering applications. Researchers have also investigated the potential of this compound in drug delivery systems, where it can serve as a biodegradable carrier for therapeutic agents.

In addition to its industrial applications, diethyl 3-aminopentanedioate has shown potential in the field of nutrition. Studies have demonstrated that this compound can act as a precursor for the synthesis of essential amino acids, which are crucial for human health. This makes it a valuable component in dietary supplements and functional foods.

Recent advancements in synthetic chemistry have led to the development of novel methods for the production of diethyl 3-aminopentanedioate. These methods include enzymatic catalysis and microwave-assisted synthesis, which offer improved yields and reduced reaction times compared to traditional techniques. The use of green chemistry principles in these methods has also contributed to the sustainability of the production process.

The biological activity of diethyl 3-aminopentanedioate has been extensively studied, particularly its role in metabolic pathways. Research has shown that this compound can influence cellular energy metabolism by modulating the activity of key enzymes involved in glycolysis and the citric acid cycle. This has implications for its potential use in treating metabolic disorders such as diabetes and obesity.

Furthermore, diethyl 3-aminopentanedioate has been explored as a chelating agent due to its ability to bind metal ions effectively. This property makes it useful in water treatment processes and as an additive in food preservatives to enhance shelf life.

In conclusion, diethyl 3-aminopentanedioate (CAS No. 60793-95-5) is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical properties and biological activity make it a subject of ongoing research interest. As advancements in synthetic methods and application development continue, this compound is poised to play an even more significant role in addressing global challenges related to health, sustainability, and material science.

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