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Catalog Number:
31798
CAS Number:
68621-88-5
N-Boc-m-phénylènediamine
Purity:
≥ 98 % (HPLC)
Synonym(s):
3-( tert -butoxycarbonylamino)aniline, tert-butyl-3-aminophénylcarbamate
Documents
$22.03 /1G
Taille
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Product Information

Conserver à l'écart des substances incompatibles, des sources d'inflammation et des agents oxydants. Éviter les périodes de stockage prolongées. Conserver sous gaz inerte (par exemple Argon)

Synonyms
3-( tert -butoxycarbonylamino)aniline, tert-butyl-3-aminophénylcarbamate
CAS Number
68621-88-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H16N2O2
Molecular Weight
208.26
MDL Number
MFCD06657915
PubChem ID
12877220
Melting Point
110 - 114 °C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
General Information
Synonyms
3-( tert -butoxycarbonylamino)aniline, tert-butyl-3-aminophénylcarbamate
CAS Number
68621-88-5
Purity
≥ 98 % (HPLC)
Molecular Formula
C11H16N2O2
Molecular Weight
208.26
MDL Number
MFCD06657915
PubChem ID
12877220
Melting Point
110 - 114 °C
Appearance
Blanc cassé uni
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-Boc-m-phenylenediamine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceutical agents, particularly in the development of drugs targeting cancer and other diseases.
  • Polymer Chemistry: It is used in the formulation of specialty polymers, enhancing properties such as thermal stability and mechanical strength, which are crucial for applications in coatings and adhesives.
  • Analytical Chemistry: Researchers employ N-Boc-m-phenylenediamine in the preparation of derivatizing agents for the analysis of amines and amino acids, improving detection sensitivity in chromatographic techniques.
  • Organic Synthesis: This compound acts as a protective group in organic synthesis, allowing for selective reactions without interfering with other functional groups, thus streamlining complex synthesis pathways.
  • Material Science: It finds application in the development of advanced materials, such as sensors and electronic devices, due to its ability to enhance conductivity and responsiveness in composite materials.

Citations