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Catalog Number:
14467
CAS Number:
430460-38-1
Ácido carboxílico 1S,2R)-Fmoc-aminociclohexano
Purity:
≥ 97 % (HPLC)
Synonym(s):
(1S,2R)-Fmoc-Achc
Documents
$168.35 /100 mg
Tamaño
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Product Information

(1S,2R)-Fmoc-aminocyclohexane carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This amino acid derivative features a protective Fmoc (9-fluorenylmethoxycarbonyl) 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 cyclohexane ring contributes to its conformational stability, enhancing the overall efficiency of peptide synthesis.

In addition to its role in peptide synthesis, (1S,2R)-Fmoc-aminocyclohexane carboxylic acid is also valuable in drug discovery and development. Its ability to facilitate the formation of peptide bonds while maintaining structural integrity makes it a preferred choice for creating bioactive peptides with potential therapeutic applications. Researchers can leverage this compound to explore new avenues in drug design, particularly in the development of peptide-based therapeutics that target specific biological pathways.

Synonyms
(1S,2R)-Fmoc-Achc
CAS Number
430460-38-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD06410975
PubChem ID
4139355
Appearance
Polvo blanco
Optical Rotation
[α] D 20 = -7 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(1S,2R)-Fmoc-Achc
CAS Number
430460-38-1
Purity
≥ 97 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD06410975
PubChem ID
4139355
Appearance
Polvo blanco
Optical Rotation
[α] D 20 = -7 ± 2º (C=1 en DMF)
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

(1S,2R)-Fmoc-aminocyclohexane carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids. Its stability under various reaction conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates by modifying amino acids to enhance bioactivity and selectivity, which is crucial for developing effective therapeutics.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Material Science: It finds applications in creating functionalized polymers and materials, contributing to advancements in smart materials that respond to environmental changes.
  • Analytical Chemistry: This chemical is also used in the preparation of standards and reagents for analytical techniques, aiding in the accurate detection and quantification of various substances in complex mixtures.

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