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Catalog Number:
16110
CAS Number:
102520-97-8
2-(boc-amino)-2-méthyl-1-propanol
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ester tert -butylique de l'acide (2-hydroxy-1,1-diméthyléthyl)carbamique, Boc-Aib-ol
Documents
$18.53 /1G
Taille
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Informations sur le produit

2-(Boc-amino)-2-methyl-1-propanol is a versatile compound widely utilized in the fields of organic synthesis and pharmaceutical development. This compound, also known as tert-butyl N-(1-hydroxy-2-methylpropan-2-yl)carbamate, serves as a valuable building block for the synthesis of various bioactive molecules. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, allows for selective reactions, making it an ideal choice for researchers looking to streamline their synthetic pathways.

In practical applications, 2-(Boc-amino)-2-methyl-1-propanol is particularly beneficial in the preparation of amino acids and peptides, which are crucial in drug discovery and development. Its stability and ease of handling further enhance its appeal, allowing for efficient processing in laboratory settings. Additionally, this compound's compatibility with various reaction conditions makes it a reliable option for chemists aiming to optimize their workflows. With its significant role in advancing research and development, 2-(Boc-amino)-2-methyl-1-propanol stands out as an essential tool for professionals in the chemical and pharmaceutical industries.

Numéro CAS 
102520-97-8
Formule moléculaire
C 9 H 19 NO 3
Poids moléculaire 
189.3
Point de fusion 
52-59 °C
Informations générales
Numéro CAS 
102520-97-8
Formule moléculaire
C 9 H 19 NO 3
Poids moléculaire 
189.3
Point de fusion 
52-59 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

2-(Boc-amino)-2-methyl-1-propanol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting the overall structure.
  • Drug Development: It is used in the pharmaceutical industry for the development of new drugs, particularly in the creation of compounds that require specific functional groups for biological activity.
  • Bioconjugation: Researchers employ this chemical in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, enhancing the efficacy of diagnostics and therapeutics.
  • Organic Synthesis: It plays a crucial role in organic synthesis, particularly in the formation of complex molecules, due to its ability to stabilize reactive intermediates.
  • Research in Medicinal Chemistry: The compound is valuable in medicinal chemistry for its role in modifying existing drugs to improve their pharmacological properties, such as solubility and bioavailability.

Citations