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Catalog Number:
04959
CAS Number:
135944-08-0
Fmoc-(DL)-2-aminotetraline-2-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-Atc-OH, (R,S-Fmoc-2-aminotetraline-2-carboxylic acid
Documents
$79.22 /250MG
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Product Information

Fmoc-(DL)-2-aminotetraline-2-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure not only enhances stability but also facilitates the formation of complex peptide chains, making it an essential building block in the pharmaceutical industry. Researchers appreciate its utility in the development of bioactive peptides, which can be employed in various therapeutic applications, including cancer treatment and neuropharmacology.

The compound's ability to provide a stable and easily removable protecting group allows for efficient synthesis processes, reducing the time and resources needed for peptide assembly. Additionally, its compatibility with various coupling reagents and methodologies makes it a preferred choice among chemists. With its significant role in advancing peptide-based therapeutics, Fmoc-(DL)-2-aminotetraline-2-carboxylic acid stands out as a key player in modern medicinal chemistry and biochemistry.

Synonyms
Fmoc-Atc-OH, (R,S-Fmoc-2-aminotetraline-2-carboxylic acid
CAS Number
135944-08-0
Purity
≥ 99% (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD00273476
PubChem ID
2733197
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-Atc-OH, (R,S-Fmoc-2-aminotetraline-2-carboxylic acid
CAS Number
135944-08-0
Purity
≥ 99% (HPLC)
Molecular Formula
C26H23NO4
Molecular Weight
413.47
MDL Number
MFCD00273476
PubChem ID
2733197
Appearance
White powder
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-(DL)-2-aminotetraline-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing drug efficacy.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, improving the delivery and effectiveness of therapeutic agents.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, helping researchers understand the mechanisms of action for various neuroactive compounds.
  • Analytical Chemistry: The compound is utilized in analytical applications, such as chromatography, to separate and identify complex mixtures, providing valuable insights in various research fields.

Citations