(Acetylmethylene)triphenylphosphorane

CAS: 1439-36-7

Ref. 3D-FA17134

Produktinformation

• Name: (Acetylmethylene)triphenylphosphorane
• Synonyme: 1-(Triphenylphosphoranylidene)-2-propanone(2-Oxopropylidene)triphenylphosphorane(Acetonylidene)triphenylphosphorane, (2-Oxopropylidene)triphenylphosphorane, (Acetonylidene)triphenylphosphorane, (Triphenylphosphoranylidene)-2-propanone, (Triphenylphosphoranylidene)acetone, 1-(Triphenyl-Lambda~5~-Phosphanylidene)Propan-2-One, 1-(Triphenyl-λ⁵-phosphanylidene)propan-2-one, 1-(Triphenylphosphanylidene)propan-2-one, 1-(Triphenylphosphoranylidene)acetone, 1-(Triphenylphosphorylidene)-2-propanone, 2-Propanone, (triphenylphosphoranylidene)-, 2-Propanone, 1-(triphenylphosphoranylidene)-, 3-(Triphenylphosphoranylidene)-2-propanone, Methyl (triphenylphosphoranylidene)methyl ketone, NSC 407394, Triphenyl(acetylmethylene)phosphorane

Beschreibung

(Acetylmethylene)triphenylphosphorane is an antibacterial agent that acts by inhibiting the synthesis of bacterial cell walls. The compound has been postulated to have a kinetic mechanism with a kinetic data derived from β-amino acid and synthetic process. This antibiotic binds to the hydroxyl group of acetic acid, which creates an unsaturated ketone. The carbonyl group of (acetylmethylene)triphenylphosphorane interacts with the phenyl groups and aldehyde groups, forming a covalent bond. This interaction prevents the formation of cross-links between peptidoglycan chains in bacterial cell walls. The antimicrobial activity of this compound is due to its ability to inhibit bacterial enzymes involved in postulated catalytic mechanism.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 318.35 g/mol
• Formel: C₂₁H₁₉OP
• Reinheit: Min. 95%
• InChl: InChI=1S/C21H19OP/c1-18(22)17-23(19-11-5-2-6-12-19,20-13-7-3-8-14-20)21-15-9-4-10-16-21/h2-17H,1H3
• InChI Key: InChIKey=KAANTNXREIRLCT-UHFFFAOYSA-N
• SMILES: CC(=O)C=P(c1ccccc1)(c1ccccc1)c1ccccc1