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Catalog Number:
31678
CAS Number:
77292-90-1
Boc-L-Ala-O-CH2-Ph-CH2-COOH
Purity:
≥ 96% (HPLC)
Documents
$43.87 /1G
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Product Information

Boc-L-Ala-O-CH2-Ph-CH2-COOH is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an ideal choice for various synthetic applications. Its unique structure allows for the selective incorporation of phenyl and acetic acid functionalities, facilitating the development of complex peptides and biologically active molecules. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound to create novel therapeutics, particularly in the design of peptide-based drugs that target specific biological pathways.

The compound's ability to undergo selective reactions while maintaining its integrity under various conditions provides significant advantages over similar compounds. Its applications extend to the synthesis of prodrugs and targeted delivery systems, showcasing its potential in advancing drug development. With its favorable properties and practical uses, Boc-L-Ala-O-CH2-Ph-CH2-COOH stands out as a valuable tool for researchers aiming to innovate in peptide chemistry and pharmaceutical formulations.

CAS Number
77292-90-1
Purity
≥ 96% (HPLC)
Molecular Formula
C17H23NO6
Molecular Weight
337.37
MDL Number
MFCD00273484
PubChem ID
14629035
Melting Point
102 - 104 ?C
Appearance
White powder
Optical Rotation
[a]20D = -30 ± 1 º (C=1 in EtOH)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
77292-90-1
Purity
≥ 96% (HPLC)
Molecular Formula
C17H23NO6
Molecular Weight
337.37
MDL Number
MFCD00273484
PubChem ID
14629035
Melting Point
102 - 104 ?C
Appearance
White powder
Optical Rotation
[a]20D = -30 ± 1 º (C=1 in EtOH)
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-Ala-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, which are crucial in developing pharmaceuticals and biologically active compounds.
  • Drug Development: It is used in the formulation of novel drug candidates, particularly in the field of targeted therapies, enhancing the efficacy of treatments.
  • Biotechnology: The compound plays a significant role in bioconjugation processes, aiding in the development of antibody-drug conjugates that improve the delivery of therapeutic agents.
  • Research in Molecular Biology: It is utilized in various biochemical assays and studies, helping researchers understand protein interactions and functions.
  • Cosmetic Formulations: The compound is also explored in the cosmetic industry for its potential in creating effective anti-aging products, leveraging its biochemical properties.

Citations