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Catalog Number:
16174
CAS Number:
264273-06-5
Acide Fmoc- trans -1,2-aminocyclohex-4-ène carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-1,2- trans -ACHeC-OH
Documents
$95.60 /250 mg
Taille
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Product Information

Fmoc-trans-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 trans configuration enhances the stability and reactivity of the cyclohexene ring, making it an ideal choice for researchers looking to create complex peptide structures with high specificity.

In the pharmaceutical industry, Fmoc-trans-1,2-aminocyclohex-4-ene carboxylic acid serves as a building block for the development of novel therapeutics, particularly in the design of cyclic peptides that exhibit improved bioactivity and stability. Its application extends to various fields, including medicinal chemistry and materials science, where it can be used to create functionalized polymers and drug delivery systems. The compound's unique properties and ease of use make it a valuable asset for researchers aiming to innovate in peptide-based applications.

Synonyms
Fmoc-1,2- trans -ACHeC-OH
CAS Number
264273-06-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 214
Molecular Weight
363.4
MDL Number
MFCD02682630
PubChem ID
20714677
Melting Point
190 - 196 °C
Appearance
Poudre cristalline blanche
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Fmoc-1,2- trans -ACHeC-OH
CAS Number
264273-06-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C 22 H 214
Molecular Weight
363.4
MDL Number
MFCD02682630
PubChem ID
20714677
Melting Point
190 - 196 °C
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-1,2-aminocyclohex-4-ene carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing chemists to build complex peptides efficiently while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is vital in developing diagnostic tools and drug delivery systems.
  • Material Science: It is applied in the development of advanced materials, such as hydrogels and polymers, which have applications in tissue engineering and regenerative medicine.
  • Research in Organic Chemistry: This chemical is a valuable intermediate in organic synthesis, allowing researchers to explore new reactions and develop innovative chemical methodologies.

Citations