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Catalog Number:
12901
CAS Number:
220497-65-4
Acide (1 R ,4 S )-(+)-4-(Fmoc-amino)-2-cyclopentène-1-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
(+)-(1 R ,4 S )- N -Fmoc-acide-4-aminocyclopent-2-ènecarboxylique
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$25.00 /25 mg
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Product Information

The compound (1R,4S)-(+)-4-(Fmoc-amino)-2-cyclopentene-1-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique cyclopentene structure that enhances its reactivity and stability, making it an excellent choice for researchers focused on developing novel peptides and drug candidates. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating streamlined synthesis processes.

In addition to its role in peptide synthesis, this compound has shown potential in the development of bioactive molecules, particularly in the fields of pharmaceuticals and biotechnology. Its structural characteristics enable the creation of diverse derivatives, which can be tailored for specific biological activities. Researchers in drug discovery can leverage this compound to explore new therapeutic avenues, making it a valuable asset in both academic and industrial laboratories.

Synonyms
(+)-(1 R ,4 S )- N -Fmoc-acide-4-aminocyclopent-2-ènecarboxylique
CAS Number
220497-65-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C 21 H 194
Molecular Weight
349.39
MDL Number
MFCD01311756
PubChem ID
2734462
Melting Point
177 - 181 ?C
Appearance
Poudre blanche
Optical Rotation
[a]23D = 11 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
(+)-(1 R ,4 S )- N -Fmoc-acide-4-aminocyclopent-2-ènecarboxylique
CAS Number
220497-65-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C 21 H 194
Molecular Weight
349.39
MDL Number
MFCD01311756
PubChem ID
2734462
Melting Point
177 - 181 ?C
Appearance
Poudre blanche
Optical Rotation
[a]23D = 11 ± 2 ° (C = 1 dans DMF)
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

(1R,4S)-(+)-4-(Fmoc-amino)-2-cyclopentene-1-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, allowing for the creation of complex structures with high purity.
  • Drug Development: Its unique cyclopentene structure makes it valuable in medicinal chemistry for developing novel pharmaceuticals, particularly those targeting specific biological pathways.
  • Bioconjugation: The Fmoc protecting group enables selective reactions, making it useful for bioconjugation applications, such as attaching drugs to antibodies for targeted therapy.
  • Research in Organic Chemistry: This compound is frequently used in organic synthesis as a versatile intermediate, allowing chemists to explore various reaction pathways and develop new methodologies.
  • Material Science: Its properties can be leveraged in the development of advanced materials, including polymers and coatings, which require specific mechanical and chemical characteristics.

Citations