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Catalog Number:
31469
CAS Number:
90965-06-3
Dimethyl (1-diazo-2-oxopropyl)phosphonate
Purity:
≥ 97% (HPLC)
Synonym(s):
Bestmann-Ohira Reagent, Dimethyl (1-azoacetonyl)phosphonate
Documents
$86.23 /1G
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Product Information

Dimethyl (1-diazo-2-oxopropyl)phosphonate is a versatile compound with significant applications in organic synthesis and chemical research. This phosphonate derivative is recognized for its ability to act as a diazo transfer agent, making it invaluable in the production of diazo compounds, which are crucial intermediates in various chemical reactions. Its unique structure allows for selective reactions, enabling chemists to create complex molecules with precision.

In the pharmaceutical industry, Dimethyl (1-diazo-2-oxopropyl)phosphonate is utilized in the synthesis of bioactive compounds, contributing to the development of new drugs and therapeutic agents. Additionally, its role in agrochemical formulations highlights its importance in creating effective pesticides and herbicides. Researchers appreciate its stability and ease of handling, which facilitate its use in laboratory settings. With its broad range of applications, this compound stands out as a key player in advancing chemical synthesis and innovation.

Synonyms
Bestmann-Ohira Reagent, Dimethyl (1-azoacetonyl)phosphonate
CAS Number
90965-06-3
Purity
≥ 97% (HPLC)
Molecular Formula
C5H9N2O4P
Molecular Weight
192.11
MDL Number
MFCD07368360
PubChem ID
53397103
Density
1.28 g/mL at 25 ?C
Appearance
Light yellow to yellow oil
Conditions
Store at 0-8 °C under inert gas.
General Information
Synonyms
Bestmann-Ohira Reagent, Dimethyl (1-azoacetonyl)phosphonate
CAS Number
90965-06-3
Purity
≥ 97% (HPLC)
Molecular Formula
C5H9N2O4P
Molecular Weight
192.11
MDL Number
MFCD07368360
PubChem ID
53397103
Density
1.28 g/mL at 25 ?C
Appearance
Light yellow to yellow oil
Conditions
Store at 0-8 °C under inert gas.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Dimethyl (1-diazo-2-oxopropyl)phosphonate is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile reagent in organic synthesis, particularly in the formation of carbon-nitrogen bonds, which are crucial for creating various pharmaceuticals and agrochemicals.
  • Pharmaceutical Development: It plays a role in drug discovery processes, enabling researchers to develop new therapeutic agents by facilitating the introduction of functional groups into drug candidates.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, due to its ability to modify chemical properties and enhance material performance.
  • Agricultural Chemistry: It is applied in the formulation of pesticides and herbicides, providing effective solutions for crop protection while minimizing environmental impact.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, aiding in the detection and quantification of other compounds, which is essential for quality control in manufacturing processes.

Citations