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Catalog Number:
33457
CAS Number:
132622-77-6
Sel de dicyclohexylamine de boc-(4 S -4-azido-D-proline)
Purity:
≥ 99 % (dosage par titration)
Synonym(s):
Boc-D-Pro(4-N3)·DCHA (2 R , 4 S, Sel de dicyclohexylamine de boc-(2 R ,4 S )-4-azidoproline
Antibiotic
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$86.23 /100 mg
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Product Information

Boc-(4S)-4-azido-D-proline dicyclohexylamine salt is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This compound features a unique azido group, which enhances its reactivity and makes it an excellent candidate for click chemistry applications, particularly in the development of bioconjugates and drug delivery systems. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating further functionalization and modification in synthetic pathways.

Researchers appreciate the compound's stability and solubility in organic solvents, making it suitable for various laboratory applications. It has been effectively employed in peptide synthesis and as an intermediate in the preparation of bioactive molecules. The dicyclohexylamine salt form enhances its handling properties, providing ease of use in laboratory settings. With its potential for diverse applications, Boc-(4S)-4-azido-D-proline dicyclohexylamine salt stands out as a valuable tool for chemists aiming to innovate in drug design and development.

Synonyms
Boc-D-Pro(4-N3)·DCHA (2 R , 4 S, Sel de dicyclohexylamine de boc-(2 R ,4 S )-4-azidoproline
CAS Number
132622-77-6
Purity
≥ 99 % (dosage par titration)
Molecular Formula
C10H16N4O4 · C12H23N
Molecular Weight
437.6
MDL Number
MFCD32067798
PubChem ID
14842620
Melting Point
144 - 150 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = 30 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Boc-D-Pro(4-N3)·DCHA (2 R , 4 S, Sel de dicyclohexylamine de boc-(2 R ,4 S )-4-azidoproline
CAS Number
132622-77-6
Purity
≥ 99 % (dosage par titration)
Molecular Formula
C10H16N4O4 · C12H23N
Molecular Weight
437.6
MDL Number
MFCD32067798
PubChem ID
14842620
Melting Point
144 - 150 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] 20 D = 30 ± 1 ° (C = 1 dans DMF)
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Oui
DEA-regulated
Non
Warnings
-
Applications

Boc-(4S)-4-azido-D-proline dicyclohexylamine salt is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of novel therapeutics. Its azido group allows for click chemistry reactions, facilitating the creation of complex peptide structures.
  • Drug Development: Researchers leverage its properties to design and optimize new drug candidates. The ability to modify the azido group opens pathways for creating targeted therapies with improved efficacy and reduced side effects.
  • Bioconjugation: The azido functionality enables bioconjugation techniques, allowing scientists to attach biomolecules to surfaces or other compounds. This is particularly useful in developing diagnostic tools and targeted drug delivery systems.
  • Material Science: In materials research, this compound can be used to create functionalized polymers. Its unique properties enhance the performance of materials in applications such as sensors and drug delivery devices.
  • Research in Chemical Biology: The compound is valuable in studying protein interactions and cellular processes. Its ability to selectively label biomolecules aids in understanding complex biological systems.

Citations