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Catalog Number:
29751
CAS Number:
36016-38-3
N -Boc-hidroxilamina
Purity:
≥ 99 % (HPLC)
Synonym(s):
N -hidroxicarbamato de terc- butilo, N- ( tert -butoxicarbonil)hidroxilamina
Documents
$18.53 /5G
Tamaño
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Product Information

Se utiliza en la preparación de azridinas por cicloadición de azidas con

Synonyms
N -hidroxicarbamato de terc- butilo, N- ( tert -butoxicarbonil)hidroxilamina
CAS Number
36016-38-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C5H11NO3
Molecular Weight
133.15
MDL Number
MFCD00002107
PubChem ID
97534
Melting Point
53-57 ?C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0-8 ºC
General Information
Synonyms
N -hidroxicarbamato de terc- butilo, N- ( tert -butoxicarbonil)hidroxilamina
CAS Number
36016-38-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C5H11NO3
Molecular Weight
133.15
MDL Number
MFCD00002107
PubChem ID
97534
Melting Point
53-57 ?C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0-8 ºC
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-Boc-hydroxylamine is widely utilized in research focused on:

  • Synthetic Chemistry: It serves as a versatile building block in the synthesis of various organic compounds, particularly in the formation of amines and amides, which are essential in pharmaceuticals and agrochemicals.
  • Drug Development: This compound is crucial in the development of prodrugs, enhancing the bioavailability of active pharmaceutical ingredients by modifying their chemical properties.
  • Analytical Chemistry: N-Boc-hydroxylamine is employed in the derivatization of carbonyl compounds, improving their detection and quantification in complex mixtures, which is vital for quality control in food and drug industries.
  • Polymer Chemistry: It is used in the preparation of functionalized polymers, contributing to the development of materials with tailored properties for applications in coatings, adhesives, and drug delivery systems.
  • Bioconjugation: The compound facilitates the conjugation of biomolecules, such as proteins and peptides, enhancing their stability and functionality for use in diagnostics and therapeutic applications.

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