CAS 7314-44-5
:2,4-Dimethoxybenzylalkohol
- (2,4-Dimethoxyphenyl)Methanol
- 2,4-Dimethoxybenzenemethanol
- 2,4-Dimethoxyphenylmethanol
- Ai3-52354
- Benzenemethanol, 2,4-dimethoxy-
- Benzyl alcohol, 2,4-dimethoxy-
- 2,4-Dimethoxybenzyl alcohol
(2,4-Dimethoxyphenyl)methanol
CAS:Formel:C9H12O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:168.18982,4-Dimethoxybenzyl alcohol
CAS:2,4-Dimethoxybenzyl alcoholFormel:C9H12O3Reinheit:≥95%Farbe und Form: white low-melting solid/ clear. colourless liquid fused solidMolekulargewicht:168.19g/mol2,4-Dimethoxybenzyl Alcohol
CAS:Formel:C9H12O3Reinheit:>98.0%(GC)Farbe und Form:White or Colorless to Almost white or Almost colorless powder to lump to clear liquidMolekulargewicht:168.192,4-Dimethoxybenzyl alcohol
CAS:2,4-Dimethoxybenzyl alcohol, an aromatic alcohol, acts as a substrate for GMC oxidoreductase with aryl-alcohol oxidase traits.Formel:C9H12O3Farbe und Form:Less To Light Yellow Liquid Colorless To Light Yellow LiquidMolekulargewicht:168.192,4-Dimethoxybenzyl alcohol
CAS:2,4-Dimethoxybenzyl alcohol is a functional group that is used in organic synthesis. It can be synthesized from the reduction of 2,4-dichlorobenzaldehyde with sodium borohydride or lithium aluminum hydride. The compound is used to synthesize hydroxamic acids and it has shown photocatalytic activity. 2,4-Dimethoxybenzyl alcohol is also used as an intermediate for the synthesis of octamers and trifluoroacetate esters. Other uses include its ability to induce chloride secretion by inhibiting the chloride ion channel in the cell membrane and its ability to inhibit quinoline derivatives such as indolocarbazoles. 2,4-Dimethoxybenzyl alcohol has been shown to have inhibitory activities against a number of biological targets including growth regulators and enzymes (i.e., stereoselective). 2,4-Dimethoxybenzyl alcohol has
Formel:C9H12O3Reinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:168.19 g/mol2,4-Dimethoxybenzyl alcohol
CAS:Formel:C9H12O3Reinheit:98%Farbe und Form:SolidMolekulargewicht:168.192






