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Catalog Number:
31705
CAS Number:
864876-78-8
Fmoc-L-Val-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 99.5% (Chiral HPLC)
Documents
$43.87 /1G
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Product Information

Fmoc-L-Val-O-CH2-Ph-OCH2-CH2-COOH is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during solid-phase peptide synthesis. Its unique structure allows for efficient coupling reactions, making it an invaluable tool for researchers in the fields of biochemistry and medicinal chemistry. The compound's ability to enhance the solubility and stability of peptides makes it particularly beneficial in the development of therapeutic agents and biologically active compounds.

In addition to its role in peptide synthesis, Fmoc-L-Val-O-CH2-Ph-OCH2-CH2-COOH is also explored for its potential applications in drug delivery systems and as a building block for complex biomolecules. Its compatibility with various coupling reagents and its favorable reactivity profile enable researchers to create diverse peptide libraries, facilitating the discovery of novel therapeutics. This compound stands out for its ease of use and effectiveness in producing high-purity peptides, making it a preferred choice among professionals in pharmaceutical and academic research settings.

CAS Number
864876-78-8
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C30H31NO7
Molecular Weight
517.58
MDL Number
MFCD08457856
PubChem ID
155893512
Appearance
White powder
Optical Rotation
[a]20D = -17 ± 1 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
864876-78-8
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C30H31NO7
Molecular Weight
517.58
MDL Number
MFCD08457856
PubChem ID
155893512
Appearance
White powder
Optical Rotation
[a]20D = -17 ± 1 º (C=1 in DMF)
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-L-Val-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Development: Its unique structure aids in the design of peptide-based therapeutics, contributing to the development of drugs that target specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, which are essential in developing targeted drug delivery systems and diagnostic tools.
  • Research in Cancer Therapy: By facilitating the synthesis of peptide analogs, it plays a role in creating potential cancer treatments that can selectively target tumor cells.
  • Protein Engineering: This chemical is valuable in modifying proteins for enhanced stability and functionality, which is crucial in various biotechnological applications.

Citations