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Catalog Number:
29936
CAS Number:
941-55-9
Solución de p -toluenosulfonil azida
Grade:
11-15 % (p/p) en tolueno
Purity:
≥ 99 % (HPLC)
Synonym(s):
Solución de azida de 4-metilbencenosulfonilo, Solución de p -toluenosulfonazida
Hazmat
Documents
$40.96 /5G
Tamaño
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Product Information

Se utiliza para la introducción de grupos funcionales azida y diazo.
También se utiliza como fuente de nitreno y como sustrato para reacciones de cicloadición [3+2].

Synonyms
Solución de azida de 4-metilbencenosulfonilo, Solución de p -toluenosulfonazida
CAS Number
941-55-9
Purity
≥ 99 % (HPLC)
Grade
11-15 % (p/p) en tolueno
Molecular Formula
C7H7N3O2S
Molecular Weight
197.21
MDL Number
MFCD00180767
PubChem ID
13661
Density
~ 0,90 g/ml a 20 °C
Appearance
Líquido incoloro a ligeramente amarillo.
Refractive Index
número 20/D 1.502
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Solución de azida de 4-metilbencenosulfonilo, Solución de p -toluenosulfonazida
CAS Number
941-55-9
Purity
≥ 99 % (HPLC)
Grade
11-15 % (p/p) en tolueno
Molecular Formula
C7H7N3O2S
Molecular Weight
197.21
MDL Number
MFCD00180767
PubChem ID
13661
Density
~ 0,90 g/ml a 20 °C
Appearance
Líquido incoloro a ligeramente amarillo.
Refractive Index
número 20/D 1.502
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
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.

Citas