AC-46989 - sodium-thiomethoxide-90-technical | 5188-07-8
Sodium thiomethoxide
CAS:Formel:CH3NaSFarbe und Form:White to yellow or brown powder or crystalsMolekulargewicht:70.09Sodium thiomethoxide solution
CAS:Sodium thiomethoxide solutionReinheit:≥95%Farbe und Form:LiquidMolekulargewicht:70.08929g/molMethyl Mercaptan Sodium Salt (ca. 15% in Water)
CAS:Formel:CH3NaSFarbe und Form:Colorless to Light orange to Yellow clear liquidMolekulargewicht:70.08Sodium methanethiolate
CAS:Sodium methanethiolateFormel:·CH3S·NaReinheit:≥95%Farbe und Form: white to off-white crystalline powderMolekulargewicht:70.08929g/molSodium Methanethiolate (~20% in Water)
CAS:Kontrolliertes ProduktApplications Strong nucleophile used for the synthesis of methyl aryl sulfides from halo-arenes. Alkanethiolates are efficient reagents for SN2 dealkylation of esters and aryl ethers.
E0
References Le Brazidec, J., et al.: J. Med. Chem., 47, 3865 (2004), Grem, J., et al.: J. Clin. Oncol., 23, 1885 (2005), Levason, W., et al.: Dalton Trans, 439 (2007),Formel:CH3S·NaFarbe und Form:ColourlessMolekulargewicht:70.09Sodium Methanethiolate (95%)
CAS:Kontrolliertes ProduktFormel:CH3S·NaReinheit:95%Farbe und Form:NeatMolekulargewicht:70.093-Methyl-2-buten-1-thiol Preparation Kit
CAS:Stability Readily Oxidized
Applications A volatile aroma compound. We will provide a detailed procedure for the preparation of the thiol from the thiolacetate with spectral data upon request.
References Majcher, M., et al.: J. Agric. Food Chem., 55, 5754 (2007), Akiyama, M., et al.: Food Sci. Technol. Res., 15, 233 (2009), Breme, K., et al.: J. Agric. Food Chem., 57, 8572 (2009),Formel:MixturepleasevisitourwebisteformoreinformationFarbe und Form:Colourless To YellowMolekulargewicht:Mixture, please visit our webiste for more informationSodium methanethiolate - 15% aqueous solution
CAS:Sodium methanethiolate is an antimicrobial agent that is a white, crystalline solid. It reacts with trifluoroacetic acid and water to produce the active form of sodium trifluoroacetate. The reaction mechanism is likely due to the formation of a bicyclic heterocycle that has been shown to be effective against a number of bacteria. Sodium methanethiolate has been used for the treatment of infectious diseases, such as respiratory infections and skin infections, as well as autoimmune diseases and cardiovascular disorders. The oxidation catalyst in this compound may also have physiological effects on the body's cells and tissues.Formel:CH3NaSReinheit:Min. 95%Farbe und Form:Clear LiquidMolekulargewicht:70.09 g/molSodium Methanethiolate-13C
CAS:Kontrolliertes ProduktApplications Sodium Methanethiolate-13C, is the labeled analogue of Sodium Methanethiolate (S644805), used as a nucleophile in organic synthesis. Sodium methanethiolate is also being used as a reagent to synthesize thiol-based suberoylanilide hydroxamic acid (SAHA) analogues, compounds that act as potent histone deacetylase inhibitors.
References Bergman, A. & Wachtmeister, Chemosphere, 7, 949 (1978); Suzuki, T.,et al.: Bioorg. Med. Chem. Lett., 14, 3313 (2004)Formel:CH3NaSReinheit:>90%Farbe und Form:NeatMolekulargewicht:71.082Sodium methanethiolate
CAS:Methanethiol is a compound that occurs naturally in the environment. It is used as a fungicide, insecticide and herbicide. Methanethiol inhibits the growth of microorganisms by binding to metal ions on the surface of cells. This prevents DNA replication and protein synthesis, leading to cell death. Methanethiol also has anti-inflammatory properties which may be due to its ability to inhibit adenosine A1 receptor activity in humans.
Formel:CH3NaSReinheit:Min. 95%Farbe und Form:White PowderMolekulargewicht:70.09 g/mol
