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Catalog Number:
30477
CAS Number:
96186-30-0
Ácido ( S )-4-(Boc-amino)-3-(Z-amino)butírico
Purity:
99 - 101% (Ensayo por titulación)
Synonym(s):
ZDb-Dbu(Boc)-OH, Ácido N b-Z- N g-Boc-S-diaminobutírico
Documents
$161.94 /100 mg
Tamaño
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Product Information

(S)-4-(Boc-amino)-3-(Z-amino)butyric acid is a versatile compound widely utilized in the fields of medicinal chemistry and peptide synthesis. This amino acid derivative features a protected amine group, making it an excellent building block for the synthesis of complex peptides and pharmaceuticals. Its unique structure allows for the introduction of various functional groups, facilitating the development of novel therapeutic agents. Researchers appreciate its stability under standard reaction conditions, which enhances its utility in various synthetic pathways.

In addition to its role in peptide synthesis, (S)-4-(Boc-amino)-3-(Z-amino)butyric acid is also employed in the development of drug candidates targeting a range of diseases, including cancer and metabolic disorders. Its ability to serve as a chiral building block allows for the creation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry. With its favorable properties and broad applicability, this compound stands out as a valuable resource for researchers and industry professionals seeking to innovate in drug development and synthesis.

Synonyms
ZDb-Dbu(Boc)-OH, Ácido N b-Z- N g-Boc-S-diaminobutírico
CAS Number
96186-30-0
Purity
99 - 101% (Ensayo por titulación)
Molecular Formula
C17H24N2O6
Molecular Weight
352.4
MDL Number
MFCD03788644
PubChem ID
3337412
Melting Point
135 - 145 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -13 a -11 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
ZDb-Dbu(Boc)-OH, Ácido N b-Z- N g-Boc-S-diaminobutírico
CAS Number
96186-30-0
Purity
99 - 101% (Ensayo por titulación)
Molecular Formula
C17H24N2O6
Molecular Weight
352.4
MDL Number
MFCD03788644
PubChem ID
3337412
Melting Point
135 - 145 °C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -13 a -11 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-4-(Boc-amino)-3-(Z-amino)butyric acid 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 drug development and biotechnology. Its unique structure allows for the introduction of specific functional groups that enhance peptide stability and activity.
  • Drug Development: In pharmaceutical research, it is used to create novel therapeutic agents. Its ability to modify amino acids makes it valuable for designing drugs that target specific biological pathways.
  • Bioconjugation: This chemical is employed in bioconjugation processes, where it helps attach biomolecules to drugs or imaging agents. This application is essential in developing targeted therapies and diagnostic tools.
  • Research on Neurotransmitters: It plays a role in studying neurotransmitter functions and interactions, particularly in neuropharmacology. Understanding these interactions can lead to advancements in treating neurological disorders.
  • Material Science: The compound is also explored in material science for creating functionalized polymers. These polymers can be used in drug delivery systems, enhancing the efficacy and specificity of treatments.

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