🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
11971
CAS Number:
147900-46-7
Acide Fmoc- trans -4-aminocyclohexane carboxylique
Purity:
≥ 97 % (dosage)
Synonym(s):
Fmoc-1,4- trans -Achc-OH, Acide Fmoc- trans -4-aminocyclohexane-1-carboxylique
Documents
$68.40 /250 mg
Taille
Request Bulk Quote
Product Information

Fmoc-trans-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 structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The compound's stability under various reaction conditions enhances its appeal in both academic and industrial settings, particularly in the fields of medicinal chemistry and biochemistry.

In addition to its role in peptide synthesis, Fmoc-trans-4-aminocyclohexane carboxylic acid can be employed in the development of novel pharmaceuticals and biologically active compounds. Its ability to facilitate the introduction of cyclohexane moieties into peptide structures opens up new avenues for the design of therapeutics with improved bioactivity and selectivity. Researchers will find this compound invaluable for advancing their projects, as it not only streamlines the synthesis process but also contributes to the creation of innovative solutions in drug discovery.

Synonyms
Fmoc-1,4- trans -Achc-OH, Acide Fmoc- trans -4-aminocyclohexane-1-carboxylique
CAS Number
147900-46-7
Purity
≥ 97 % (dosage)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD01862343
PubChem ID
2756173
Melting Point
210 - 230 °C (déc.)
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-1,4- trans -Achc-OH, Acide Fmoc- trans -4-aminocyclohexane-1-carboxylique
CAS Number
147900-46-7
Purity
≥ 97 % (dosage)
Molecular Formula
C 22 H 234
Molecular Weight
365.4
MDL Number
MFCD01862343
PubChem ID
2756173
Melting Point
210 - 230 °C (déc.)
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-trans-4-aminocyclohexane carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing for the efficient assembly of peptides with specific sequences.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in designing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, improving the functionality of diagnostic and therapeutic agents.
  • Material Science: It is applied in the creation of advanced materials, such as hydrogels, which can be used in drug delivery systems and tissue engineering.
  • Research in Organic Chemistry: This compound is valuable in organic synthesis research, providing a versatile framework for exploring new chemical reactions and methodologies.

Citations