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Catalog Number:
47705
CAS Number:
642091-68-7
1-Azido-3,6,9-trioxaundécan-11-Boc-amine
Purity:
≥ 97%
Synonym(s):
N3 - PEG(3)-NH-Boc, BocNH - PEG3 - CH2CH2N3
Documents
$40.00 /25 mg
Taille
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Product Information

Il est utilisé comme lieur Click-chemistry dans diverses applications, par exemple dans la construction du lieur HyT5.

Synonyms
N3 - PEG(3)-NH-Boc, BocNH - PEG3 - CH2CH2N3
CAS Number
642091-68-7
Purity
≥ 97%
Molecular Formula
C13H26N4O5
Molecular Weight
318.4
MDL Number
MFCD22056317
Appearance
Huile incolore
Conditions
Conserver à ≤ -15 °C
General Information
Synonyms
N3 - PEG(3)-NH-Boc, BocNH - PEG3 - CH2CH2N3
CAS Number
642091-68-7
Purity
≥ 97%
Molecular Formula
C13H26N4O5
Molecular Weight
318.4
MDL Number
MFCD22056317
Appearance
Huile incolore
Conditions
Conserver à ≤ -15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1-Azido-3,6,9-trioxaundecan-11-Boc-amine is widely utilized in research focused on:

  • Drug Development: This compound serves as a versatile building block in the synthesis of pharmaceutical agents, particularly in the development of novel drug candidates with enhanced efficacy.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies and diagnostics.
  • Polymer Chemistry: The compound is used in the formulation of advanced polymers, providing unique properties such as increased stability and functionality, which are essential in materials science.
  • Click Chemistry: Its azide functional group makes it an ideal candidate for click chemistry reactions, facilitating the rapid and efficient synthesis of complex molecular structures.
  • Surface Modification: This chemical is applied in modifying surfaces for improved biocompatibility in medical devices, enhancing their performance and safety in clinical applications.

Citations