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Catalog Number:
11954
CAS Number:
147900-45-6
Acide Fmoc -cis- 4-aminocyclohexane carboxylique
Purity:
≥ 97 % (HPLC)
Synonym(s):
Fmoc-1,4- cis -Achc-OH, Acide Fmoc- cis -4-aminocyclohexane-1-carboxylique
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Product Information

Fmoc-cis-4-aminocyclohexane carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique cis configuration enhances its stability and reactivity, making it an ideal choice for researchers focused on developing novel therapeutic peptides. The compound's ability to facilitate the formation of complex structures allows for the exploration of new drug candidates with improved efficacy and reduced side effects.

In addition to its applications in peptide synthesis, Fmoc-cis-4-aminocyclohexane carboxylic acid is also valuable in the field of materials science, where it can be used to create functionalized polymers and advanced materials. Its compatibility with various coupling reagents and its ease of deprotection make it a preferred choice among chemists. Researchers can leverage this compound to streamline their synthesis processes, ultimately accelerating the development of innovative solutions in pharmaceuticals and materials engineering.

Synonyms
Fmoc-1,4- cis -Achc-OH, Acide Fmoc- cis -4-aminocyclohexane-1-carboxylique
CAS Number
147900-45-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD01862344
PubChem ID
2756173
Melting Point
130 - 138 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-1,4- cis -Achc-OH, Acide Fmoc- cis -4-aminocyclohexane-1-carboxylique
CAS Number
147900-45-6
Purity
≥ 97 % (HPLC)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD01862344
PubChem ID
2756173
Melting Point
130 - 138 ?C
Appearance
Poudre 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-cis-4-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, particularly in solid-phase peptide synthesis (SPPS). Its Fmoc protecting group allows for easy deprotection, streamlining the process of creating complex peptides.
  • Drug Development: In pharmaceutical research, it is used to develop new drug candidates, especially in the creation of cyclic peptides that can exhibit enhanced biological activity and stability.
  • Bioconjugation: The compound can be employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in drug delivery systems and diagnostics.
  • Material Science: It finds applications in the development of novel materials, such as hydrogels and polymers, which can be tailored for specific uses in biomedical devices or drug release systems.
  • Research in Organic Chemistry: Researchers utilize this compound to explore reaction mechanisms and develop new synthetic methodologies, benefiting from its unique structural features that can influence reactivity.

Citations