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Catalog Number:
29639
CAS Number:
488761-06-4
R-Fmoc-2-amino-3-phenylsulfanyl-propionic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-L-Cys(phenyl)-OH
Documents
$60.49 /25MG
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Product Information

(R)-Fmoc-2-amino-3-phenylsulfanyl-propionic acid is a valuable 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 the synthesis of peptides. Its unique structure, characterized by the presence of a phenylsulfanyl group, enhances the compound's reactivity and stability, making it an excellent choice for researchers focused on developing novel therapeutic peptides.

In practical applications, (R)-Fmoc-2-amino-3-phenylsulfanyl-propionic acid serves as a key building block in the synthesis of bioactive peptides, which are crucial in pharmaceuticals and biotechnology. Its ability to facilitate the formation of disulfide bonds in peptide chains allows for the creation of more complex and functional molecules. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for its efficiency in streamlining peptide synthesis processes, ultimately leading to faster development timelines for new drugs and therapies.

Synonyms
Fmoc-L-Cys(phenyl)-OH
CAS Number
488761-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO4S
Molecular Weight
419.5
MDL Number
MFCD08063325
PubChem ID
11316089
Appearance
White powder
Optical Rotation
[a]D20 = -58 ± 2º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Cys(phenyl)-OH
CAS Number
488761-06-4
Purity
≥ 98% (HPLC)
Molecular Formula
C24H21NO4S
Molecular Weight
419.5
MDL Number
MFCD08063325
PubChem ID
11316089
Appearance
White powder
Optical Rotation
[a]D20 = -58 ± 2º (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

(R)-Fmoc-2-amino-3-phenylsulfanyl-propionic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a crucial building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the efficient assembly of complex peptide sequences.
  • Drug Development: It plays a significant role in the pharmaceutical industry for developing novel therapeutics, especially in creating peptide-based drugs that can target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to other biomolecules, enhancing the delivery and efficacy of drugs or imaging agents in targeted therapies.
  • Research in Neuroscience: It is employed in studies related to neurotransmitter systems, helping researchers understand the role of specific peptides in neural signaling and potential implications for treating neurological disorders.
  • Protein Engineering: This chemical is beneficial in the field of protein engineering, where it aids in modifying proteins to improve their stability and functionality for various industrial applications.

Citations