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Catalog Number:
16172
CAS Number:
1212305-88-8
Fmoc-cis-1,2-aminocyclohex-4-ene carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-1,2-cis-ACHeC-OH
Documents
$141.41 /250MG
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Product Information

Fmoc-cis-1,2-aminocyclohex-4-ene carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its cis configuration and cyclohexene structure contribute to its stability and reactivity, making it an ideal choice for researchers looking to create complex peptide sequences with high specificity.

In the pharmaceutical industry, Fmoc-cis-1,2-aminocyclohex-4-ene carboxylic acid is particularly valuable for developing novel therapeutics, as it can facilitate the incorporation of non-standard amino acids into peptide chains. This capability enhances the diversity of peptide libraries, which is crucial for drug discovery and development. Additionally, its favorable solubility and compatibility with various coupling reagents make it a preferred choice for chemists aiming to streamline their synthesis processes.

Synonyms
Fmoc-1,2-cis-ACHeC-OH
CAS Number
1212305-88-8
Purity
≥ 98% (HPLC)
Molecular Formula
C22H21NO4
Molecular Weight
363.4
MDL Number
MFCD02682628
PubChem ID
20714677
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-1,2-cis-ACHeC-OH
CAS Number
1212305-88-8
Purity
≥ 98% (HPLC)
Molecular Formula
C22H21NO4
Molecular Weight
363.4
MDL Number
MFCD02682628
PubChem ID
20714677
Appearance
White crystalline powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-cis-1,2-aminocyclohex-4-ene carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the incorporation of unique structural features that enhance biological activity.
  • Drug Development: Its ability to modify amino acids makes it valuable in the pharmaceutical industry for designing new drugs with improved efficacy and reduced side effects.
  • Bioconjugation: The Fmoc group provides a protective mechanism that facilitates the attachment of biomolecules, aiding in the development of targeted therapies and diagnostic tools.
  • Material Science: It is used in the creation of advanced materials, such as hydrogels, which have applications in tissue engineering and regenerative medicine.
  • Research in Organic Chemistry: This compound is a useful reagent in various organic synthesis reactions, enabling researchers to explore new chemical pathways and reactions.

Citations