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Catalog Number:
08095
CAS Number:
32221-83-3
Formyl-L-alanine methyl ester
Purity:
≥ 98% (TLC)
Synonym(s):
For-L-Ala-OMe
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Product Information

Formyl-L-alanine methyl ester is a versatile compound widely recognized for its applications in peptide synthesis and pharmaceutical research. This compound, also known as methyl (2S)-2-formamidopropanoate, serves as a valuable building block in the development of bioactive molecules and therapeutic agents. Its unique structure allows for the introduction of formyl and methyl ester functionalities, making it an essential intermediate in the synthesis of various amino acid derivatives and peptides. Researchers appreciate its role in enhancing the solubility and stability of compounds, which is crucial in drug formulation and development.

In addition to its significance in synthetic chemistry, formyl-L-alanine methyl ester is utilized in the study of enzyme mechanisms and protein interactions. Its ability to participate in various chemical reactions, including acylation and amidation, opens up pathways for innovative research in medicinal chemistry and biochemistry. The compound's favorable properties, such as its reactivity and compatibility with diverse reaction conditions, make it an ideal choice for researchers looking to explore new therapeutic avenues.

Synonyms
For-L-Ala-OMe
CAS Number
32221-83-3
Purity
≥ 98% (TLC)
Molecular Formula
C5H9NO3
Molecular Weight
131.13
MDL Number
MFCD00080914
PubChem ID
10307863
Appearance
Clear, yellow liquid
Conditions
Store at 0-8 °C
General Information
Synonyms
For-L-Ala-OMe
CAS Number
32221-83-3
Purity
≥ 98% (TLC)
Molecular Formula
C5H9NO3
Molecular Weight
131.13
MDL Number
MFCD00080914
PubChem ID
10307863
Appearance
Clear, yellow liquid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Formyl-L-alanine methyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, crucial for developing pharmaceuticals and biologically active compounds.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Analytical Chemistry: The compound plays a role in analytical applications, such as chromatography, where it helps in the separation and identification of amino acids and peptides.
  • Drug Development: In medicinal chemistry, it aids in designing new drugs by modifying existing compounds to improve efficacy and reduce side effects.
  • Research in Metabolism: It is utilized in studies related to amino acid metabolism, providing insights into metabolic pathways and potential therapeutic targets.

Citations