CAS 1445-45-0
:1,1,1-Triméthoxyéthane
- 1,1,1-Triethoxyethane
- 1,1,1-Trimethoxy-Ethan
- Ethane, 1,1,1-trimethoxy-
- Methyl orthoacetate
- Orthoacetic acid, trimethyl ester
- Trimethyl Orthoacetate (TMOA)
- Trimethyl orthoacetate
- 1,1,1-Trimethoxyethane
- TMOA
- trimethyl-acetate
- TrimethoxyOrthoAcetate
- Methylorthoformic acid trimethyl ester
- Trimethylorthoacetat
- CH3C(OCH3)3
- Trimethylorthoaceate
- Voir plus de synonymes
Trimethyl Orthoacetate
CAS :Formule :C5H12O3Degré de pureté :>98.0%(GC)Couleur et forme :Colorless clear liquidMasse moléculaire :120.15Trimethyl orthoacetate, 98%
CAS :Trimethyl orthoacetate is used as a diols can be protected as their 1-methoxyethylidene cyclic acetals (2-methoxy-2-methyl-1,3-dioxolanes) by acid-catalyzed exchange. It is mainly used as the chemical intermediates of the medicine. Some of the other applications includes it is mainly used as chemi
Formule :C5H12O3Degré de pureté :98%Couleur et forme :Liquid, Clear colorless to pale yellowMasse moléculaire :120.15Trimethyl orthoacetate
CAS :Formule :C5H12O3Degré de pureté :(GC) ≥ 98.5%Couleur et forme :Clear, colourless liquidMasse moléculaire :120.15Trimethyl Orthoacetate
CAS :Produit contrôléApplications Trimethyl Orthoacetate is used as a reagent in the synthesis of Pseudomonic Acid D Sodium (P839520); an antibiotic isolated from Pseudomonas fluorescens.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Banks, R.M., et al.: J. Antibiot., 41, 609 (1988); Sridhar, Y., et al.: Org. Biomol. Chem., 12, 2950 (2014)Formule :C5H12O3Couleur et forme :NeatMasse moléculaire :120.151,1,1-Trimethoxyethane
CAS :Formule :C5H12O3Degré de pureté :95.0%Couleur et forme :Liquid, ClearMasse moléculaire :120.148Trimethyl orthoacetate
CAS :Trimethyl orthoacetate is a reactive chemical compound that reacts with alkanoic acids to produce esters. It is a colorless liquid at room temperature and has a pleasant odor. Trimethyl orthoacetate can be used in the synthesis of esters, which are important intermediates in the development of pharmaceuticals and agrochemicals. The reaction mechanism of trimethyl orthoacetate has been studied by means of matrix effect and kinetic energy analysis, showing that it is an exothermic reaction. This chemical reacts with water to form hydrogen gas and acetone, which can be dangerous if it occurs on an industrial scale. Trimethyl orthoacetate also acts as a glp-1r agonist, which regulates blood sugar levels, and as such might have potential use in the treatment of type 2 diabetes mellitus.
Formule :C5H12O3Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :120.15 g/mol






