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Catalog Number:
29595
CAS Number:
153039-17-9
Acide boc-4-amino-2,2-diméthyl-butyrique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 4-( tert -butoxycarbonylamino)-2,2-diméthylbutanoïque
Documents
$58.39 /100 mg
Taille
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Product Information

Boc-4-amino-2,2-dimethyl-butyric acid is a versatile compound widely utilized in the synthesis of peptides and pharmaceutical intermediates. This amino acid derivative features a tert-butoxycarbonyl (Boc) protecting group, which is crucial for the selective protection of amines during chemical reactions. Its unique structure allows for enhanced stability and solubility, making it an ideal choice for researchers engaged in drug development and peptide synthesis. The compound's ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino group is particularly advantageous in the production of complex biomolecules.

In addition to its role in peptide synthesis, Boc-4-amino-2,2-dimethyl-butyric acid is also employed in various applications within the fields of medicinal chemistry and biochemistry. Its properties make it suitable for use in the development of therapeutic agents, particularly in the design of inhibitors and modulators. Researchers appreciate its compatibility with a range of coupling reagents, which enhances its utility in diverse synthetic pathways. Overall, this compound stands out for its effectiveness in facilitating complex organic transformations, making it a valuable asset in both academic and industrial settings.

Synonyms
Acide 4-( tert -butoxycarbonylamino)-2,2-diméthylbutanoïque
CAS Number
153039-17-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 21 NON 4
Molecular Weight
231.29
MDL Number
MFCD04038508
PubChem ID
4306222
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide 4-( tert -butoxycarbonylamino)-2,2-diméthylbutanoïque
CAS Number
153039-17-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 21 NON 4
Molecular Weight
231.29
MDL Number
MFCD04038508
PubChem ID
4306222
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-4-amino-2,2-dimethyl-butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions that enhance the yield and purity of the final product.
  • Pharmaceutical Development: It is used in the design of drug candidates, particularly in the development of amino acid derivatives that can lead to novel therapeutic agents.
  • Biotechnology: The compound plays a role in the modification of biomolecules, aiding in the creation of more effective biopharmaceuticals with improved stability and bioavailability.
  • Material Science: It is incorporated into polymer chemistry for producing specialty polymers with tailored properties, which can be applied in coatings and adhesives.
  • Research Applications: This chemical is valuable in academic and industrial research settings for studying the structure-activity relationships of amino acids and their derivatives.

Citations