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Catalog Number:
31694
CAS Number:
111623-14-4
Boc-L-Tyr(2-Br-Z)-O-CH2-Ph-CH2-COOH
Purity:
≥ 98% (HPLC)
Documents
$72.31 /1G
Pack Size Availability Price
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Product Information

Boc-L-Tyr(2-Br-Z)-O-CH2-Ph-CH2-COOH is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical industry for its ability to enhance the stability and bioavailability of peptide-based therapeutics. The presence of the bromine atom and the Boc (tert-butyloxycarbonyl) protecting group allows for selective reactions, making it an excellent choice for researchers looking to develop complex peptide structures with improved pharmacological properties.

In addition to its applications in drug formulation, Boc-L-Tyr(2-Br-Z)-O-CH2-Ph-CH2-COOH is also utilized in the synthesis of various bioactive compounds, including those targeting specific receptors in cancer therapy. Its unique structure facilitates the design of novel therapeutic agents, providing researchers with a versatile tool for advancing medicinal chemistry. With its combination of stability and reactivity, this compound stands out as a valuable resource for both academic and industrial applications in the field of biochemistry.

CAS Number
111623-14-4
Purity
≥ 98% (HPLC)
Molecular Formula
C31H32BrNO9
Molecular Weight
642.5
MDL Number
MFCD00273521
PubChem ID
155894051
Melting Point
100-105 ?C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
CAS Number
111623-14-4
Purity
≥ 98% (HPLC)
Molecular Formula
C31H32BrNO9
Molecular Weight
642.5
MDL Number
MFCD00273521
PubChem ID
155894051
Melting Point
100-105 ?C
Appearance
White powder
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-L-Tyr(2-Br-Z)-O-CH2-Ph-CH2-COOH 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 therapeutic agents. Its unique structure allows for the incorporation of brominated tyrosine, enhancing the biological activity of peptides.
  • Drug Development: It is employed in the pharmaceutical industry for designing novel drugs, especially in oncology. The bromine substitution can improve the compound's interaction with biological targets, potentially leading to more effective treatments.
  • Bioconjugation: The compound is useful in bioconjugation processes, where it can be linked to other biomolecules, such as antibodies or enzymes, to create targeted delivery systems for drugs or imaging agents.
  • Research in Neuroscience: Its application in neuroscience research is notable, as it can be used to study the effects of modified amino acids on neurotransmitter systems, providing insights into neurological disorders.
  • Analytical Chemistry: The compound is also valuable in analytical chemistry for developing assays that require specific interactions with proteins or enzymes, aiding in the detection and quantification of biomolecules.

Citations