CAS 6443-69-2
:3,4,5-Trimethoxytoluol
- 1,2,3-Trimethoxy-5-methylbenzene
- 1-Methyl-3,4,5-trimethoxybenzene
- 2,6-Dimethoxy-4-methylanisole
- 3,4,5-Trimethoxy toluene
- 3,4,5-Trimethoxy-1-methylbenzene
- 5-Methyl-1,2,3-trimethoxybenzene
- 5-Methylpyrogallol trimethyl ether
- Benzene, 1,2,3-trimethoxy-5-methyl-
- Toluene, 3,4,5-trimethoxy-
- 3,4,5-Trimethoxytoluene
- 3,4,5-Trimethoxytolune
- 5-METHYL PYROGALLOL TRIMETHYL ETHER
- Benzene, 5-methyl-1,2,3-trimethoxy
- Weitere Synonyme anzeigen
3,4,5-Trimethoxytoluene
CAS:Formel:C10H14O3Reinheit:>98.0%(GC)Farbe und Form:White or Colorless to Light yellow powder to lump to clear liquidMolekulargewicht:182.223,4,5-Trimethoxytoluene, 98%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formel:C10H14O3Reinheit:98%Farbe und Form:Colorless to white, Crystals or powder or crystalline powder or lumpsMolekulargewicht:182.223,4,5-Trimethoxytoluene
CAS:Formel:C10H14O3Reinheit:98%Farbe und Form:Liquid, LumpsMolekulargewicht:182.219(3,4,5-Trimethoxy)toluene
CAS:Trimethoxytoluene is a natural phenolic compound that is found in the medicinal plant Aristolochia clematitis. Trimethoxytoluene has been shown to have an inhibitory effect on the reaction of phthalic anhydride and nitrobenzene. It reacts with acidic phs to form aristolochic acid, which prevents nucleophilic attack on the aromatic ring. Trimethoxytoluene also inhibits the Friedel-Crafts reaction by reacting with the alkylating agent, benzoyl chloride, which forms a complex that cannot react further. The reaction products are biphenyl and 3,4,5-trimethoxybenzyl alcohol. Trimethoxytoluene is converted into vitamin D3 when exposed to ultraviolet light.
Formel:C10H14O3Reinheit:Min. 95%Molekulargewicht:182.22 g/mol3,4,5-Trimethoxytoluene
CAS:Applications 3,4,5-Trimethoxytoluene is a reagent for oxadiazolylindazole sodium channel modulators which are neuroprotective toward hippocampal neurons.
References Clutterbuck, L. A., et al.: J. Med. Chem., 52, 2694 (2009);Formel:C10H14O3Farbe und Form:NeatMolekulargewicht:182.22






