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Catalog Number:
22709
CAS Number:
946761-08-6
Acide 4-Boc-amino-tétrahydrothiopyran-4-yl)acétique
Purity:
≥ 99 % (HPLC)
Documents
$100.05 /25 mg
Taille
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Product Information

(4-Boc-amino-tetrahydrothiopyran-4-yl)acetic acid is a versatile compound that plays a significant role in pharmaceutical and chemical research. This compound, also known as 4-Boc-amino-thian-4-yl acetic acid, features a unique tetrahydrothiopyran structure that enhances its potential as a building block in the synthesis of various bioactive molecules. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, making it an ideal candidate for peptide synthesis and medicinal chemistry applications.

Researchers and industry professionals can leverage (4-Boc-amino-tetrahydrothiopyran-4-yl)acetic acid in the development of novel therapeutic agents, particularly in the fields of drug discovery and development. Its ability to facilitate the introduction of amino acids into complex molecular frameworks opens up new avenues for creating targeted therapies. Additionally, its stability and compatibility with various reaction conditions make it a valuable asset in synthetic organic chemistry, providing a reliable option for those looking to streamline their synthesis processes.

CAS Number
946761-08-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 21 NON 4 S
Molecular Weight
275.36
MDL Number
MFCD09264197
PubChem ID
17040198
Melting Point
142-160 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8°C
General Information
CAS Number
946761-08-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 12 H 21 NON 4 S
Molecular Weight
275.36
MDL Number
MFCD09264197
PubChem ID
17040198
Melting Point
142-160 ?C
Appearance
Poudre blanche
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

(4-Boc-amino-tetrahydrothiopyran-4-yl)acetic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of novel pharmaceuticals, particularly those targeting neurological disorders, due to its unique structural properties.
  • Peptide Synthesis: It is used in the preparation of peptide-based drugs, enhancing the stability and bioavailability of therapeutic peptides, which is crucial in drug formulation.
  • Bioconjugation: The compound can be employed in bioconjugation processes, linking biomolecules for targeted drug delivery systems, improving the efficacy of treatments.
  • Research in Organic Chemistry: It acts as a versatile building block in organic synthesis, allowing chemists to create complex molecules with specific functionalities.
  • Analytical Chemistry: This chemical is utilized in analytical methods for the detection and quantification of thiol-containing compounds, aiding in various biochemical analyses.

Citations