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Catalog Number:
15257
CAS Number:
220497-83-6
Fmoc-D-α-(5-bromothienyl)alanine
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-D-2-(5-bromothienyl)alanine
Documents
$45.00 /100MG
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Product Information

Fmoc-D-a-(5-bromothienyl)alanine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound features a unique bromothienyl group, which enhances its utility in various applications, particularly in the field of medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing stability during synthesis. Researchers often utilize this compound in the development of novel peptides with potential therapeutic applications, including anti-cancer and anti-inflammatory agents.

The distinct properties of Fmoc-D-a-(5-bromothienyl)alanine make it an attractive choice for scientists looking to explore structure-activity relationships in drug discovery. Its ability to facilitate the introduction of thienyl moieties into peptide sequences opens new avenues for the design of bioactive compounds. Moreover, its compatibility with standard solid-phase peptide synthesis techniques ensures that it can be seamlessly integrated into existing workflows, making it a valuable addition to any research laboratory focused on peptide chemistry.

Synonyms
Fmoc-D-2-(5-bromothienyl)alanine
CAS Number
220497-83-6
Purity
≥ 97% (HPLC)
Molecular Formula
C22H18BrNO4S
Molecular Weight
472.35
MDL Number
MFCD01311772
PubChem ID
22571998
Appearance
White solid
Optical Rotation
[a]D25 = 23 ± 2 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-2-(5-bromothienyl)alanine
CAS Number
220497-83-6
Purity
≥ 97% (HPLC)
Molecular Formula
C22H18BrNO4S
Molecular Weight
472.35
MDL Number
MFCD01311772
PubChem ID
22571998
Appearance
White solid
Optical Rotation
[a]D25 = 23 ± 2 ° (C=1 in DMF)
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

Fmoc-D-a-(5-bromothienyl)alanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis. Its Fmoc protecting group allows for easy removal under mild conditions, making it ideal for creating complex peptide structures.
  • Drug Development: The unique bromothienyl moiety enhances the biological activity of peptides, making it valuable in the pharmaceutical industry for developing new drugs with improved efficacy and selectivity.
  • Bioconjugation: It can be used in bioconjugation techniques to attach peptides to various biomolecules, facilitating the creation of targeted therapies and diagnostic agents in medical research.
  • Fluorescent Probes: The compound can be incorporated into fluorescent probes, allowing researchers to visualize and track peptide interactions in live cells, which is crucial for understanding cellular processes.
  • Material Science: Its unique properties make it suitable for developing advanced materials, such as conducting polymers and sensors, which can be applied in electronics and environmental monitoring.

Citations