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Catalog Number:
15081
CAS Number:
389057-34-5
Ácido carboxílico Fmoc-(1 R ,2 R -2-aminociclohexano
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-( 1R ,2R - ACHC-OH
Documents
$114.37 /100 mg
Tamaño
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Product Information

Fmoc-(1R,2R)-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 crucial for the selective protection of amino groups during the synthesis of peptides. Its unique cyclohexane structure enhances the conformational flexibility of peptides, making it an ideal choice for researchers aiming to develop novel therapeutics with improved bioactivity and stability.

In addition to its application in peptide synthesis, Fmoc-(1R,2R)-2-aminocyclohexane carboxylic acid is also valuable in the development of chiral ligands and catalysts, contributing to advancements in asymmetric synthesis. The compound's ability to facilitate the formation of complex molecular architectures positions it as a key reagent in the pharmaceutical industry, particularly in the design of drugs targeting various biological pathways. Researchers and industry professionals can leverage this compound to enhance their synthetic strategies and achieve higher yields in their projects.

Synonyms
Fmoc-( 1R ,2R - ACHC-OH
CAS Number
389057-34-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD05663770
PubChem ID
4139355
Appearance
Polvo o sólido blanco
Optical Rotation
[a] D 20 = -34 ± 2º (C=1 en acetona) o
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-( 1R ,2R - ACHC-OH
CAS Number
389057-34-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD05663770
PubChem ID
4139355
Appearance
Polvo o sólido blanco
Optical Rotation
[a] D 20 = -34 ± 2º (C=1 en acetona) o
Conditions
Conservar entre 0 y 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-(1R,2R)-2-aminocyclohexane carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions while preventing unwanted side reactions. Its stability under various conditions makes it a preferred choice for chemists.
  • Drug Development: In pharmaceutical research, it is used to create cyclic peptide libraries, aiding in the discovery of new drug candidates with enhanced biological activity and specificity.
  • Bioconjugation: The compound is instrumental in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostic and therapeutic agents.
  • Material Science: It finds applications in the development of functional materials, particularly in creating polymeric systems that require specific interactions or properties, such as drug delivery systems.
  • Research in Chiral Catalysis: Its chiral nature makes it valuable in studies focused on asymmetric synthesis, where it can help improve the selectivity and yield of desired products in chemical reactions.

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