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Catalog Number:
31393
CAS Number:
15263-20-4
N-(tert-Butoxycarbonyloxy)phthalimide
Purity:
≥ 99% (HPLC)
Synonym(s):
tert-Butyl Phthalimido Carbonate
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Product Information

N-(tert-Butoxycarbonyloxy)phthalimide is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound, also known as tert-butyl phthalimide, serves as an effective protecting group for amines, facilitating the selective functionalization of complex molecules. Its unique structure allows for easy cleavage under mild conditions, making it an ideal choice for chemists looking to streamline their synthetic pathways.

In addition to its role in organic synthesis, N-(tert-Butoxycarbonyloxy)phthalimide has shown promise in the development of various pharmaceutical agents, particularly in the synthesis of biologically active compounds. Researchers appreciate its stability and compatibility with a range of reaction conditions, which enhances its utility in both academic and industrial settings. The compound's ability to improve yields and simplify purification processes makes it a valuable asset in the toolkit of synthetic chemists and pharmaceutical developers alike.

Synonyms
tert-Butyl Phthalimido Carbonate
CAS Number
15263-20-4
Purity
≥ 99% (HPLC)
Molecular Formula
C13H13NO5
Molecular Weight
263.25
MDL Number
MFCD00005889
PubChem ID
84857
Melting Point
116.5-118.5 ?C
Appearance
Off-white to white crystalline powder
Conditions
Store at 2-8 °C
General Information
Synonyms
tert-Butyl Phthalimido Carbonate
CAS Number
15263-20-4
Purity
≥ 99% (HPLC)
Molecular Formula
C13H13NO5
Molecular Weight
263.25
MDL Number
MFCD00005889
PubChem ID
84857
Melting Point
116.5-118.5 ?C
Appearance
Off-white to white crystalline powder
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-(tert-Butoxycarbonyloxy)phthalimide is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile protecting group for amines in organic synthesis, allowing chemists to selectively modify other functional groups without affecting the amine.
  • Pharmaceutical Development: It is used in the synthesis of pharmaceutical intermediates, providing a means to create complex molecules with high specificity, which is crucial in drug formulation.
  • Polymer Chemistry: The compound can be employed in the production of specialty polymers, enhancing properties such as thermal stability and mechanical strength, making it valuable in materials science.
  • Bioconjugation: In biochemistry, it facilitates the conjugation of biomolecules, aiding in the development of targeted drug delivery systems and improving therapeutic efficacy.
  • Analytical Chemistry: It is utilized as a reagent in various analytical techniques, helping researchers to identify and quantify compounds in complex mixtures, thus streamlining the analysis process.

Citations