742724

Dimethyl (1-diazo-2-oxopropyl)phosphonate solution

~10% in acetonitrile (H-NMR), ≥96% (HPLC)

• Sinónimos: Bestmann-Ohira Reagent, Dimethyl (1-azoacetonyl)phosphonate solution, Dimethyl (acetyldiazomethyl)phosphonate solution
• Fórmula empírica (notación de Hill): C₅H₉N₂O₄P
• Número de CAS: 90965-06-3
• Peso molecular: 192.11
• Beilstein/REAXYS Number: 4247670
• MDL number: MFCD07368360
• UNSPSC Code: 12352108
• PubChem Substance ID: 329765588
• NACRES: NA.22

Propiedades

• assay: ≥96% (HPLC)
• form: liquid
• reaction suitability: reaction type: C-C Bond Formation
• concentration: ~10% in acetonitrile (H-NMR)
• refractive index: n20/D 1.352-1.354
• density: 0.800-0.850 g/mL at 20 °C
• functional group: ketone; phosphonate
• storage temp.: 2-8°C
• SMILES string: COP(=O)(OC)C(=[N+]=[N-])C(C)=O
• InChI: 1S/C5H9N2O4P/c1-4(8)5(7-6)12(9,10-2)11-3/h1-3H3
• InChI key: SQHSJJGGWYIFCD-UHFFFAOYSA-N

Descripción

Application

Dimethyl (1-diazo-2-oxopropyl)phosphonate can be used as a reagent for the synthesis of:

• Ethynyl compounds (alkynes) from aldehydes.
• Isoquinoline and pyridine N-oxides by cyclization with oximes in the presence of Rh catalyst.
• Dimethyl(diazomethyl)phosphonate through methanolysis, which is further employed as a reagent in the synthesis of enol ethers or alkynes.
• Five-member heterocyclic scaffolds of pyrazoles, triazoles, and oxazoles via cycloaddition reaction and multicomponent reaction.

Información de seguridad

• pictograms: GHS02,GHS07
• signalword: Danger
• hcodes: H225,H302 + H312 + H332,H319
• pcodes: P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P312 - P305 + P351 + P338
• Hazard Classifications: Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
• Storage Class: 3 - Flammable liquids
• wgk_germany: WGK 3
• flash_point_f: 35.6 °F
• flash_point_c: 2 °C