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Catalog Number:
03733
CAS Number:
111524-95-9
Fmoc-D-phenylglycine
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-D-Phg-OH, (R)-Fmoc-2-aminophenylacetic acid
Documents
$22.03 /1G
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Product Information
Synonyms
Fmoc-D-Phg-OH, (R)-Fmoc-2-aminophenylacetic acid
CAS Number
111524-95-9
Purity
≥ 99% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.4
MDL Number
MFCD00190891
PubChem ID
3702842
Melting Point
168 - 182 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -81 ± 3 º (C=1% in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-D-Phg-OH, (R)-Fmoc-2-aminophenylacetic acid
CAS Number
111524-95-9
Purity
≥ 99% (HPLC)
Molecular Formula
C23H19NO4
Molecular Weight
373.4
MDL Number
MFCD00190891
PubChem ID
3702842
Melting Point
168 - 182 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -81 ± 3 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-D-phenylglycine is widely utilized in research focused on

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide structures efficiently.
  • Drug Development: It plays a significant role in medicinal chemistry, where it is used to design and develop new pharmaceutical compounds, particularly those targeting specific biological pathways.
  • Bioconjugation: Fmoc-D-phenylglycine can be employed in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: This compound is used in studies related to neurotransmitter systems, helping researchers understand the role of peptides in neural signaling and potential therapeutic applications.
  • Protein Engineering: It is valuable in the field of protein engineering, where it aids in the modification of proteins to enhance their stability and activity, offering advantages over other amino acid derivatives.

Citations