Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
26440
CAS Number:
179251-60-6
Ácido N α -Boc- N β -aloxicarbonil-D-2,3-diaminopropiónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-D-Dap(Aloc)-OH
Documents
$79.22 /1G
Tamaño
Request Bulk Quote
Product Information

Na-Boc-Nb-allyoxycarbonyl-D-2,3-diaminopropionic acid is a versatile compound widely utilized in the field of organic synthesis and peptide chemistry. This compound features a unique structure that enhances its reactivity and compatibility with various coupling reactions, making it an essential building block for the synthesis of complex peptides and bioactive molecules. Its protective Boc (tert-butyloxycarbonyl) group allows for selective deprotection, facilitating the introduction of functional groups in a controlled manner.

Researchers and industry professionals can leverage Na-Boc-Nb-allyoxycarbonyl-D-2,3-diaminopropionic acid in the development of pharmaceuticals, particularly in the design of peptide-based drugs and therapeutic agents. Its ability to serve as a chiral building block opens avenues for the synthesis of enantiomerically pure compounds, which are crucial in drug development. Additionally, its stability under various reaction conditions makes it an attractive option for both academic research and industrial applications, ensuring high yields and purity in the final products.

Synonyms
Boc-D-Dap(Aloc)-OH
CAS Number
179251-60-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H20N2O6
Molecular Weight
288.3
MDL Number
MFCD05663724
PubChem ID
3593591
Melting Point
87-93 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +12 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-D-Dap(Aloc)-OH
CAS Number
179251-60-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H20N2O6
Molecular Weight
288.3
MDL Number
MFCD05663724
PubChem ID
3593591
Melting Point
87-93 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +12 ± 2º (C=1 en MeOH)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Nb-allyoxycarbonyl-D-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of novel pharmaceuticals, particularly in creating compounds with enhanced bioavailability and stability.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is applied in studies involving neurotransmitter systems, helping researchers explore potential therapeutic agents for neurological disorders.
  • Material Science: The compound is utilized in the development of advanced materials, particularly in creating polymers with specific properties for industrial applications.

Citas