CAS 5779-95-3
:3,5-Dimetil benzaldeído
- M-xylene-5-carboxaldehyde
- Benzaldehyde, 3,5-dimethyl-
- 3,5-Dimethylbenzaldehyde
3,5-Dimethylbenzaldehyde
CAS:Fórmula:C9H10OPureza:>96.0%(GC)Cor e Forma:Colorless to Light yellow to Light orange clear liquidPeso molecular: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
Fórmula:C9H10OPureza:98%Cor e Forma:Clear colorless, LiquidPeso molecular:134.183,5-Dimethylbenzaldehyde
CAS:3,5-Dimethylbenzaldehyde has broad-spectrum antimicrobial activity, inhibiting Bacillus subtilis, Pseudomonas albicans, Escherichia coli, Pseudomonas aeruginosaFórmula:C9H10OPureza:99.4%Cor e Forma:SolidPeso molecular: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
Fórmula:C9H10OPureza:Min. 95%Cor e Forma:Colorless Clear LiquidPeso molecular:134.18 g/mol






