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Catalog Number:
15082
CAS Number:
312965-07-4
Fmoc-(1S,2S)-2-aminocyclohexane carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-(1S,2S)-Achc-OH
Documents
$95.00 /100MG
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Product Information

Fmoc-(1S,2S)-2-aminocyclohexane carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing novel peptides and bioactive compounds. The compound's stability under various reaction conditions enhances its applicability in complex synthetic pathways, providing a reliable option for both academic and industrial laboratories.

In addition to its role in peptide synthesis, Fmoc-(1S,2S)-2-aminocyclohexane carboxylic acid has potential applications in drug discovery and development, particularly in the design of cyclic peptides and peptidomimetics. Its ability to facilitate the introduction of stereochemistry into peptide sequences opens up new avenues for creating therapeutics with improved efficacy and selectivity. Researchers can leverage this compound to explore innovative solutions in fields such as oncology, immunology, and infectious diseases, making it a valuable asset in the pharmaceutical industry.

Synonyms
Fmoc-(1S,2S)-Achc-OH
CAS Number
312965-07-4
Purity
≥ 98% (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD05663771
PubChem ID
4139355
Appearance
White to off-white solid
Optical Rotation
[a]20D = +47.5 ± 2 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-(1S,2S)-Achc-OH
CAS Number
312965-07-4
Purity
≥ 98% (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD05663771
PubChem ID
4139355
Appearance
White to off-white solid
Optical Rotation
[a]20D = +47.5 ± 2 º (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-(1S,2S)-2-aminocyclohexane carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of specific amino acid sequences that are crucial for biological activity.
  • Drug Development: It plays a significant role in the pharmaceutical industry, particularly in the design of novel drugs that target specific receptors, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies related to neurobiology, where its structural properties aid in the design of compounds that can cross the blood-brain barrier, potentially leading to new treatments for neurological disorders.
  • Material Science: This chemical is also explored in the development of advanced materials, such as polymers and nanomaterials, due to its unique chemical properties that enhance material performance.

Citations