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Catalog Number:
31680
CAS Number:
73401-72-6
Boc-L-Asn-O-CH2-Ph-CH2-COOH
Purity:
≥ 95% (HPLC)
Documents
$43.87 /1G
Pack Size Availability Price
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Product Information

Boc-L-Asn-O-CH2-Ph-CH2-COOH is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and facilitates the selective functionalization of the amino group during synthesis. Its unique structure allows for the incorporation of phenyl and acetic acid moieties, making it an excellent choice for developing complex peptides and biologically active molecules. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound to create novel therapeutic agents, particularly in the development of targeted drug delivery systems and enzyme inhibitors.

The compound's ability to serve as a building block in the synthesis of peptide-based drugs highlights its significance in pharmaceutical applications. Its stability under various conditions and compatibility with standard coupling reagents make it an ideal candidate for both academic and industrial research settings. By integrating Boc-L-Asn-O-CH2-Ph-CH2-COOH into their workflows, professionals can streamline their synthesis processes and enhance the efficacy of their peptide-based products.

CAS Number
73401-72-6
Purity
≥ 95% (HPLC)
Molecular Formula
C18H24N2O7
Molecular Weight
380.4
MDL Number
MFCD00273488
PubChem ID
3419448
Melting Point
165-170 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -8 ± 1° (C=1 in EtOH)
Conditions
Store at 0-8 °C
General Information
CAS Number
73401-72-6
Purity
≥ 95% (HPLC)
Molecular Formula
C18H24N2O7
Molecular Weight
380.4
MDL Number
MFCD00273488
PubChem ID
3419448
Melting Point
165-170 ?C
Appearance
White powder
Optical Rotation
[a]D20 = -8 ± 1° (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-Asn-O-CH2-Ph-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a versatile building block in the synthesis of peptides, allowing researchers to create complex structures for drug development and biological studies.
  • Drug Development: Its unique structure facilitates the design of novel pharmaceuticals, particularly in the field of targeted therapies, enhancing the efficacy of treatments.
  • Bioconjugation: The compound is used in bioconjugation processes, where it can be linked to proteins or antibodies, improving the specificity and effectiveness of therapeutic agents.
  • Research in Neuroscience: It plays a role in studying neurotransmitter pathways, aiding researchers in understanding neurological disorders and developing potential treatments.
  • Cosmetic Formulations: The compound is also explored in cosmetic chemistry for its potential to improve skin penetration of active ingredients, enhancing product effectiveness.

Citations