CAS 5779-95-3
:3,5-Dimethyl benzaldehyde
- M-xylene-5-carboxaldehyde
- Benzaldehyde, 3,5-dimethyl-
- 3,5-Dimethylbenzaldehyde
3,5-Dimethylbenzaldehyde
CAS:Formula:C9H10OPurity:>96.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:134.183,5-Dimethylbenzaldehyde, 98%
CAS:3,5-Dimethylbenzaldehyde is used to produce 2,3-bis-(3,5-dimethyl-phenyl)-succinonitrile by heating along with reagent NaCN and solvent H2O, methanol. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may
Formula:C9H10OPurity:98%Color and Shape:Clear colorless, LiquidMolecular weight:134.183,5-Dimethylbenzaldehyde
CAS:3,5-Dimethylbenzaldehyde has broad-spectrum antimicrobial activity, inhibiting Bacillus subtilis, Pseudomonas albicans, Escherichia coli, Pseudomonas aeruginosaFormula:C9H10OPurity:99.4%Color and Shape:SolidMolecular weight:134.183,5-Dimethylbenzaldehyde
CAS:3,5-Dimethylbenzaldehyde is an organic compound that is a colorless liquid. It has a chemical formula of C9H12O2 and is classified as an aldehyde. 3,5-Dimethylbenzaldehyde can be synthesized by the reaction of isopropyl palmitate with xylene in the presence of carbon as a source. The reaction time required for this synthesis is approximately one day. The major products of this reaction are 3,5-dimethylbenzaldehyde and 2-methylbutanal. This reaction mechanism can also be used to determine the concentration of urinary metabolites in human urine samples. Analysis of these samples requires an organic solvent such as hexane or dichloromethane. Kinetic data was collected from the rate at which zinc powder reacts with 3,5-dimethylbenzaldehyde over time at different concentrations. A kinetic experiment was conducted using c–h bond activation to produce 3,5-dimethoxy
Formula:C9H10OPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:134.18 g/mol






