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Catalog Number:
29333
CAS Number:
55418-27-4
O-(2-Fluorobenzyl)hydroxylamine
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Product Information

O-(2-Fluorobenzyl)hydroxylamine is a versatile chemical compound recognized for its unique properties and applications in various fields, particularly in organic synthesis and pharmaceutical research. This compound serves as an effective reagent in the preparation of hydroxylamine derivatives, which are crucial in the synthesis of amines and other nitrogen-containing compounds. Its ability to selectively react with carbonyl compounds makes it invaluable in the development of pharmaceuticals, agrochemicals, and fine chemicals. Researchers appreciate its role in facilitating the formation of oximes, which are essential intermediates in the synthesis of numerous bioactive molecules.

Additionally, O-(2-Fluorobenzyl)hydroxylamine's fluorine substitution enhances its reactivity and selectivity, providing advantages over similar compounds in specific applications. This feature allows for more efficient synthesis pathways, reducing the need for extensive purification processes. Its utility in medicinal chemistry, particularly in the design of novel drug candidates, highlights its relevance in contemporary research. With its practical applications and unique properties, O-(2-Fluorobenzyl)hydroxylamine stands out as a valuable tool for researchers and industry professionals alike.

CAS Number
55418-27-4
Molecular Formula
C7H8FNO
Molecular Weight
141.14
MDL Number
MFCD11594365
PubChem ID
468123
Conditions
Store at 0-8°C
General Information
CAS Number
55418-27-4
Molecular Formula
C7H8FNO
Molecular Weight
141.14
MDL Number
MFCD11594365
PubChem ID
468123
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

O-(2-Fluorobenzyl)hydroxylamine is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting neurological disorders.
  • Analytical Chemistry: It is used in the derivatization of carbonyl compounds, enhancing their detection in analytical methods such as gas chromatography and mass spectrometry.
  • Organic Synthesis: The compound acts as a versatile reagent in organic synthesis, facilitating the formation of amines and other nitrogen-containing compounds, which are essential in many chemical processes.
  • Biochemical Research: Researchers utilize it to study enzyme mechanisms and interactions, particularly those involving nitrogen species, contributing to a deeper understanding of metabolic pathways.
  • Material Science: It is employed in the development of novel materials, particularly in creating polymers with specific functional properties, enhancing their performance in various applications.

Citations