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Catalog Number:
16173
CAS Number:
381241-08-3
Acide Fmoc- trans -2-aminocyclohexanecarboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-1,2- trans- ACHC-OH
Documents
$110.70 /250 mg
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Product Information

Fmoc-trans-2-aminocyclohexanecarboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which provides stability during the synthesis process while allowing for selective deprotection. Its trans configuration enhances the steric accessibility of the amino group, making it an ideal choice for the development of cyclic peptides and other complex structures. Researchers appreciate its ability to facilitate the introduction of chirality into peptide sequences, which is crucial for the design of biologically active compounds.

In addition to its role in peptide synthesis, Fmoc-trans-2-aminocyclohexanecarboxylic acid has shown potential in drug discovery and development, particularly in the creation of inhibitors and modulators for various biological targets. Its unique properties enable chemists to explore new avenues in therapeutic applications, including cancer treatment and antimicrobial agents. With its proven track record in enhancing the efficacy of peptide-based drugs, this compound stands out as a valuable asset for researchers and industry professionals alike.

Synonyms
Fmoc-1,2- trans- ACHC-OH
CAS Number
381241-08-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD02682626
PubChem ID
4139355
Melting Point
190-196 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-1,2- trans- ACHC-OH
CAS Number
381241-08-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD02682626
PubChem ID
4139355
Melting Point
190-196 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-trans-2-aminocyclohexanecarboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure makes it valuable in the design of new pharmaceuticals, particularly in creating compounds that can effectively target specific biological pathways.
  • Bioconjugation: It is used in bioconjugation processes to link biomolecules, enhancing the stability and efficacy of therapeutic agents.
  • Research in Neuroscience: This chemical is applied in studies related to neuropeptides, helping researchers understand their role in neurological functions and disorders.
  • Custom Synthesis: Laboratories often utilize it for custom synthesis projects, enabling the creation of tailored compounds for specific research needs.

Citations