Cas no 3078-36-2 (2-Amino-3-(1H-pyrrol-2-yl)propanoic acid)

2-Amino-3-(1H-pyrrol-2-yl)propanoic acid is a non-proteinogenic amino acid featuring a pyrrole moiety, which confers unique chemical and biological properties. Its structural characteristics make it valuable as a building block in peptide synthesis and medicinal chemistry, particularly for designing analogs with enhanced binding affinity or selectivity. The pyrrole ring offers potential for π-stacking interactions and metal coordination, expanding its utility in catalysis and material science. This compound is also of interest in biochemical research due to its potential role as a precursor or intermediate in specialized metabolic pathways. High-purity grades ensure reproducibility in synthetic applications, while its stability under standard conditions facilitates handling and storage.
2-Amino-3-(1H-pyrrol-2-yl)propanoic acid structure
3078-36-2 structure
Product Name:2-Amino-3-(1H-pyrrol-2-yl)propanoic acid
CAS No:3078-36-2
MF:C7H10N2O2
MW:154.166501522064
MDL:MFCD09841939
CID:916190
PubChem ID:17817718
Update Time:2025-05-20

2-Amino-3-(1H-pyrrol-2-yl)propanoic acid Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-3-(1H-pyrrol-2-yl)propanoic acid
    • 3-(2-Pyrrolyl)-DL-alanine
    • 2-amino-3-pyrrol-2-yl-propionic acid
    • 3-< Pyrrolyl-(2)> -alanin
    • AG-A-50748
    • AGN-PC-01M5PZ
    • ANW-52567
    • CTK7I4466
    • SureCN5298353
    • alpha-Amino-1H-pyrrole-2-propanoic acid
    • 2-Amino-3-(1H-pyrrol-2-yl)-propionic acid
    • EN300-318200
    • 3-(1H-Pyrrol-2-yl)alanine
    • DB-293508
    • Z1065645554
    • SB36502
    • A857612
    • 3078-36-2
    • SCHEMBL5298353
    • MFCD09841939
    • DTXSID10591095
    • CS-0005389
    • AKOS012261648
    • 1H-Pyrrole-2-propanoic acid, alpha-amino-
    • 2-Amino-3-(1H-pyrrol-2-yl)propanoicacid
    • MDL: MFCD09841939
    • Inchi: 1S/C7H10N2O2/c8-6(7(10)11)4-5-2-1-3-9-5/h1-3,6,9H,4,8H2,(H,10,11)
    • InChI Key: REBWUCRWJNKVLL-UHFFFAOYSA-N
    • SMILES: OC(C(CC1=CC=CN1)N)=O

Computed Properties

  • Exact Mass: 154.0743
  • Monoisotopic Mass: 154.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 3
  • Complexity: 149
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.6
  • Topological Polar Surface Area: 79.1?2

Experimental Properties

  • Density: 1.331
  • Boiling Point: 351.5°C at 760 mmHg
  • Flash Point: 166.4°C
  • Refractive Index: 1.606
  • PSA: 79.11

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Additional information on 2-Amino-3-(1H-pyrrol-2-yl)propanoic acid

Compound CAS No 3078-36-2: 2-Amino-3-(1H-pyrrol-2-yl)propanoic Acid

Compound CAS No 3078-36-2, also known as 2-Amino-3-(1H-pyrrol-2-yl)propanoic acid, is a fascinating organic compound with a unique structure and diverse applications. This compound has garnered significant attention in recent years due to its potential in various fields, including pharmaceuticals, materials science, and biotechnology. In this article, we will delve into the properties, synthesis, applications, and the latest research findings related to this compound.

The molecular structure of 2-Amino-3-(1H-pyrrol-2-yl)propanoic acid consists of a pyrrole ring attached to a propanoic acid backbone with an amino group. This arrangement imparts the compound with both acidic and basic properties, making it versatile for various chemical reactions. The pyrrole ring is a key feature of this molecule, contributing to its reactivity and ability to participate in hydrogen bonding. Recent studies have highlighted the importance of this structure in drug design, particularly in the development of bioactive compounds with potential therapeutic applications.

One of the most notable aspects of Compound CAS No 3078-36-2 is its synthesis. Researchers have developed several methods to synthesize this compound, including condensation reactions and enzymatic approaches. The choice of synthesis method depends on the desired purity and scale of production. For instance, a study published in *Journal of Organic Chemistry* demonstrated a novel enzymatic route that significantly improved the yield and efficiency of the synthesis process. This advancement has opened new avenues for large-scale production of this compound for industrial applications.

The applications of 2-Amino-3-(1H-pyrrol-2-yl)propanoic acid are vast and continually expanding. In the pharmaceutical industry, this compound serves as a building block for synthesizing bioactive molecules with potential anti-inflammatory, antioxidant, and anticancer properties. Recent research has shown that derivatives of this compound exhibit promising activity against various cancer cell lines, making it a valuable candidate for drug discovery programs.

In addition to its pharmaceutical applications, Compound CAS No 3078-36-2 has found uses in materials science. Its ability to form stable complexes with metal ions makes it an ideal candidate for developing coordination polymers and metalloorganic frameworks (MOFs). A study published in *Nature Materials* highlighted the use of this compound in creating highly porous MOFs with exceptional gas adsorption capabilities. These materials have potential applications in gas storage, catalysis, and environmental remediation.

Another emerging application of 2-Amino-3-(1H-pyrrol-2-yli)propanoic acid is in biotechnology. Its ability to act as a chelating agent has made it useful in metalloenzyme mimicry and biosensor development. Researchers have successfully utilized this compound to design biosensors capable of detecting heavy metal ions in environmental samples with high sensitivity and selectivity.

Despite its numerous advantages, handling Compound CAS No 3078-36_ requires caution due to its chemical reactivity. Proper safety measures must be taken during synthesis and handling to prevent exposure to hazardous conditions. Storage should be done in a cool, dry place away from incompatible materials.

In conclusion, Compound CAS No 3078_ - also known as 2-Amino_ - has proven to be a versatile and valuable compound with wide-ranging applications across multiple disciplines. Ongoing research continues to uncover new uses and improve existing methods for its synthesis and application. As technology advances, we can expect even more innovative uses for this remarkable molecule in the future.

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