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Catalog Number:
16175
CAS Number:
1217650-00-4
Fmoc-trans-1,4-aminocyclohexaneacetic acid
Purity:
≥ 99% (Assay by titration, HPLC)
Synonym(s):
Fmoc-1,4-trans-ACHA-OH
Documents
$80.00 /250MG
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Product Information

Fmoc-trans-1,4-aminocyclohexaneacetic 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 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 focusing on the development of complex peptides and pharmaceuticals.

The compound's stability and compatibility with various coupling reagents enhance its utility in solid-phase peptide synthesis, enabling the production of high-purity peptides for therapeutic applications. Additionally, its trans configuration contributes to favorable steric properties, which can improve the biological activity of the resulting peptides. Researchers in medicinal chemistry and biochemistry will find Fmoc-trans-1,4-aminocyclohexaneacetic acid invaluable for advancing their projects, particularly in the design of peptide-based drugs and biomolecules.

Synonyms
Fmoc-1,4-trans-ACHA-OH
CAS Number
1217650-00-4
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C23H25NO4
Molecular Weight
379.4
MDL Number
MFCD04973171
PubChem ID
4094934
Melting Point
191 - 198 °C
Appearance
White crystalline powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-1,4-trans-ACHA-OH
CAS Number
1217650-00-4
Purity
≥ 99% (Assay by titration, HPLC)
Molecular Formula
C23H25NO4
Molecular Weight
379.4
MDL Number
MFCD04973171
PubChem ID
4094934
Melting Point
191 - 198 °C
Appearance
White crystalline powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-trans-1,4-aminocyclohexaneacetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, enhancing the efficiency and selectivity of peptide formation.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating compounds with improved bioavailability and target specificity.
  • Bioconjugation: Researchers use it for bioconjugation applications, allowing for the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic development.
  • Material Science: The compound is applied in the development of advanced materials, such as hydrogels, which are used in drug delivery systems and tissue engineering.
  • Research in Neuroscience: It aids in the synthesis of compounds that interact with neurotransmitter systems, facilitating studies on neurological disorders and drug interactions.

Citations