Dimethyl acetylmethylphosphonate

CAS : 4202-14-6

Ref. 3D-FD61619

Informations sur le produit

• Nom: Dimethyl acetylmethylphosphonate
• Synonymes: (2-Oxopropyl)phosphonic acid dimethyl ester, (Dimethylphosphono)acetone, 1-Dimethoxyphosphorylpropan-2-one, Acetylmethylphosphonic acid dimethyl ester~Dimethyl acetonylphosphonate~Dimethyl (2-oxopropyl)phosphonate, Dimethyl 2-oxopropanephosphonate, Dimethyl 2-oxopropylphosphonate, Dimethyl P-(2-oxopropyl)phosphonate, Dimethyl acetonylphosphonate, Dimethyl β-keto-propylphosphonate, Phosphonic acid, (2-oxopropyl)-, dimethyl ester, Phosphonic acid, P-(2-oxopropyl)-, dimethyl ester, Phosphonic acid, acetonyl-, dimethyl ester

Description

Dimethyl acetylmethylphosphonate is a chlorinated organocatalytic reagent that is used in the Friedel-Crafts reaction. It can be used as an acceptor in the synthesis of pharmaceutical formulations and has been shown to react with chloride, triethyl orthoformate, 4-acetamidobenzenesulfonyl azide, β-unsaturated ketone, hexahydrate, trifluoromethanesulfonic acid, c1-4 alkyl aldehydes, and phosphonates.
The Friedel-Crafts reaction is an organic reaction that involves the conversion of an unsaturated compound into another compound with more double bonds by adding a hydrogen atom to one of the carbons in the molecule. This process can be used for many purposes such as creating drugs or other chemicals. Dimethyl acetylmethylphosphonate is an example of a chemical that can be synthesized using this reaction.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 166.11 g/mol
• Formule: C₅H₁₁O₄P
• Degré de pureté: Min. 95%
• Couleur/Forme: Colourless To Yellow To Light Brown Liquid
• InChI: InChI=1S/C5H11O4P/c1-5(6)4-10(7,8-2)9-3/h4H2,1-3H3
• Code InChI: InChIKey=UOWIYNWMROWVDG-UHFFFAOYSA-N
• SMILES: COP(=O)(CC(C)=O)OC