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Catalog Number:
29936
CAS Number:
941-55-9
Solution d'azoture de p -toluènesulfonyle
Grade:
11-15 % (p/p) dans le toluène
Purity:
≥ 99 % (HPLC)
Synonym(s):
Solution d'azoture de 4-méthylbenzènesulfonyle, Solution de p -toluènesulfonazide
Hazmat
Documents
$40.96 /5G
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Product Information

Utilisé pour l'introduction de groupes fonctionnels azotures et diazo.
Il est également utilisé comme source de nitrène et comme substrat pour les réactions de cycloaddition [3+2].

Synonyms
Solution d'azoture de 4-méthylbenzènesulfonyle, Solution de p -toluènesulfonazide
CAS Number
941-55-9
Purity
≥ 99 % (HPLC)
Grade
11-15 % (p/p) dans le toluène
Molecular Formula
C7H7N3O2S
Molecular Weight
197.21
MDL Number
MFCD00180767
PubChem ID
13661
Density
~ 0,90 g/mL à 20 °C
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20/D 1.502
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Solution d'azoture de 4-méthylbenzènesulfonyle, Solution de p -toluènesulfonazide
CAS Number
941-55-9
Purity
≥ 99 % (HPLC)
Grade
11-15 % (p/p) dans le toluène
Molecular Formula
C7H7N3O2S
Molecular Weight
197.21
MDL Number
MFCD00180767
PubChem ID
13661
Density
~ 0,90 g/mL à 20 °C
Appearance
Liquide incolore à légèrement jaune
Refractive Index
n20/D 1.502
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

p-Toluenesulfonyl azide solution is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the synthesis of various azides and enabling the formation of nitrogen-containing compounds, which are essential in pharmaceuticals and agrochemicals.
  • Click Chemistry: It plays a crucial role in click chemistry reactions, particularly in the synthesis of bioconjugates. Researchers can use it to create stable linkages between biomolecules, enhancing drug delivery systems and diagnostic tools.
  • Material Science: The compound is employed in developing new materials, such as polymers and coatings, that require specific functional groups. Its ability to introduce azide functionalities allows for further modifications, leading to innovative applications in electronics and nanotechnology.
  • Medicinal Chemistry: In drug discovery, it is used to create bioactive compounds through the introduction of azide groups, which can improve the pharmacological properties of potential drug candidates.
  • Analytical Chemistry: This solution is also utilized in analytical methods, such as mass spectrometry, to help identify and quantify various compounds in complex mixtures, providing valuable data for researchers in environmental and clinical studies.

Citations