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Catalog Number:
04933
CAS Number:
161453-37-8
Boc-3-(2'-quinolyl)-L-alanine
Purity:
≥ 99% (TLC)
Synonym(s):
Boc-L-Ala(2'-quinolyl)-OH, Boc-(S-2-amino-3-quinolin-2-yl-propionic acid
Documents
$50.30 /25MG
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Product Information

Boc-3-(2'-quinolyl)-L-alanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and usability in various chemical reactions. Its unique quinoline moiety not only contributes to its structural complexity but also imparts potential biological activity, making it a valuable building block for the development of bioactive peptides and pharmaceuticals. Researchers have utilized Boc-3-(2'-quinolyl)-L-alanine in the synthesis of targeted drug candidates, particularly in the fields of cancer research and neuropharmacology, where its ability to modulate biological pathways is of great interest.

The compound's favorable solubility and compatibility with a range of coupling reagents make it an ideal choice for peptide coupling reactions. Its application extends to the synthesis of peptide-based therapeutics, where the incorporation of quinoline derivatives has shown promise in enhancing the efficacy and selectivity of drug candidates. With its unique properties and practical applications, Boc-3-(2'-quinolyl)-L-alanine is an essential tool for researchers aiming to innovate in drug design and development.

Synonyms
Boc-L-Ala(2'-quinolyl)-OH, Boc-(S-2-amino-3-quinolin-2-yl-propionic acid
CAS Number
161453-37-8
Purity
≥ 99% (TLC)
Molecular Formula
C17H20N2O4
Molecular Weight
316.3
MDL Number
MFCD00671380
PubChem ID
4520053
Melting Point
155-159º C
Appearance
White powder
Optical Rotation
-22.50º ± 1º (c=1% in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Ala(2'-quinolyl)-OH, Boc-(S-2-amino-3-quinolin-2-yl-propionic acid
CAS Number
161453-37-8
Purity
≥ 99% (TLC)
Molecular Formula
C17H20N2O4
Molecular Weight
316.3
MDL Number
MFCD00671380
PubChem ID
4520053
Melting Point
155-159º C
Appearance
White powder
Optical Rotation
-22.50º ± 1º (c=1% in MeOH)
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

Boc-3-(2'-quinolyl)-L-alanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require specific structural features for biological activity. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: It plays a significant role in medicinal chemistry, particularly in the design of new pharmaceuticals targeting various diseases. The quinoline moiety can enhance the biological properties of drug candidates, making them more effective.
  • Biochemical Research: Researchers utilize this compound to study protein interactions and enzyme activities, providing insights into cellular mechanisms and potential therapeutic targets.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography and mass spectrometry, to identify and quantify biological samples, ensuring accurate results in research and quality control.
  • Material Science: Its unique properties make it suitable for developing advanced materials, such as sensors and coatings, which can be tailored for specific applications in electronics and environmental monitoring.

Citations