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Catalog Number:
05612
CAS Number:
80971-82-0
Boc-O-acetyl-L-tyrosine
Purity:
≥ 98%
Synonym(s):
Boc-L-Tyr(Ac)-OH
Documents
$74.81 /1G
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Product Information

Boc-O-acetyl-L-tyrosine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and pharmaceutical research. This compound, known for its protective Boc (tert-butyloxycarbonyl) group, enhances the stability and solubility of peptides during synthesis, making it an essential building block for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure allows for selective modifications, facilitating the development of novel therapeutic agents and biologically active compounds.

In addition to its applications in peptide synthesis, Boc-O-acetyl-L-tyrosine is also utilized in the production of various bioactive molecules, including those targeting neurological disorders and cancer. Its acetyl group contributes to improved lipophilicity, which can enhance the bioavailability of drug candidates. Researchers appreciate its ease of use and compatibility with standard coupling reagents, making it an ideal choice for those looking to streamline their synthetic processes while achieving high yields and purity.

Synonyms
Boc-L-Tyr(Ac)-OH
CAS Number
80971-82-0
Purity
≥ 98%
Molecular Formula
C16H21NO6
Molecular Weight
323.35
MDL Number
MFCD00057973
PubChem ID
19079949
Melting Point
80 - 85 °C
Appearance
Off-white powder
Optical Rotation
[a]20D = 11 ± 1 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Tyr(Ac)-OH
CAS Number
80971-82-0
Purity
≥ 98%
Molecular Formula
C16H21NO6
Molecular Weight
323.35
MDL Number
MFCD00057973
PubChem ID
19079949
Melting Point
80 - 85 °C
Appearance
Off-white powder
Optical Rotation
[a]20D = 11 ± 1 º (C=1 in MeOH)
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

Boc-O-acetyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of pharmaceuticals and biologically active compounds.
  • Drug Development: Its acetyl and Boc protecting groups enhance the stability and solubility of drug candidates, making it valuable in the formulation of new medications.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, which is crucial in targeted therapies.
  • Research in Neuroscience: As a derivative of tyrosine, it plays a role in studies related to neurotransmitter synthesis, aiding researchers in understanding neurological disorders.
  • Protein Engineering: Its unique structure allows for modifications in protein design, facilitating advancements in enzyme activity and stability for industrial applications.

Citations