Dibenzyl Ketone is used as a solvent and an intermediate in the synthesis of pharmaceuticals and pesticides. PubChem Substance ID 24893606.
Dibenzyl ketone or 13-diphenylacetone is an organic compound composed of two benzyl groups attached to a central carbonyl group.
Dibenzyl ketone. This results in the central carbonyl carbon atom being electrophilic and the two adjacent carbon atoms slightly nucleophilic. Molecular Weight 21027. This medication is used to treat high blood pressure and heavy sweating due to a certain tumor of the adrenal glands pheochromocytoma.
That dibenzyl ketone is formed in greater yields than Phenylacetone is evidence that reaction 3 has a greater reaction rate than reaction 2. Due to the carbanion like nature of enolates they can add to carbonyls in a similar manner as Grignard reagents. BeilsteinREAXYS Number 974767.
1 Structures Expand this section. May cause an allergic skin reaction Warning Sensitization SkinH400 9811. The noted result that the percent cage is the same at low field and at ultrahigh fields is interpreted to mean that a new mechanism spin-orbit coupling dominates the reversible singlet –.
13-Diphenylacetone Dibenzyl ketone CAS Number 102-04-5. Linear Formula C 6 H 5 CH 2 2 CO. 4 Spectral Information Expand this section.
13-diphenylacetonedibenzyl ketone13-diphenyl-2-propanonebenzyl ketone2-propanone 13-diphenyl13-diphenylpropanonealphaalpha-diphenylacetone13-diphenyl-propan-2-oneunii-9y07g5udkqfema no. Edit article at Wikipedia. Phenoxybenzamine belongs to a class of drugs known as alpha.
The fundamental transformation in this reaction is a dimerization of an aldehyde or ketone to a beta-hydroxy aldehyde or ketone by alpha CH addition of one reactant molecule to the carbonyl group of a second reactant molecule. Very toxic to aquatic life Warning Hazardous to the aquatic environment acute hazardH410 9811. 172515 Synthetic flavoring substances and adjuvants.
Sweet powdery and honey with floral rose nuances. 2 Names and Identifiers Expand this section. Dibenzyl ketone or 13-diphenylacetone is an organic compound composed of two benzyl groups attached to a central carbonyl group.
This results in the central carbonyl carbon atom being electrophilic and the two adjacent carbon atoms slightly nucleophilic. The hydrothermal decomposition reactions of the model ketone dibenzyl ketone form a mixture of reduction dehydration fragmentation and coupling products that suggest simultaneous and competitive radical and ionic reaction pathways. For this reason dibenzyl ketone is frequently used in an aldol condensation reaction with benzil a dicarbonyl and base to create tetraphenylcyclopentadienone.
3 Chemical and Physical Properties Expand this section. Triplet intersystem crossing in molecules. Dibenzyl ketone and phenyibenzyl ketones were studied as prototypes and data are tabulated for magnetic field effects in the cage reactions of para-monosubstituted dibenzyl ketones.
TCC 11000 C. At 1000 in ethyl alcohol. Diaminomaleonitrile Benzyl fluoride Alpha and beta carbon and more.
Very toxic to aquatic life with long lasting effects Warning Hazardous to the aquatic environment long-term hazardPrecautionary Statement Codes. Phenylacetone and Dibenzyl Ketone evidently are pyrolytic products of phenylacetic acetic anhydride and phenylacetic anhydride respectively. Dibenzyl ketone is similar to these topics.