CAS 5188-07-8
:Metanotiolato de sodio
Descripción:
Metanotiolato de sodio, con el número CAS 5188-07-8, es un compuesto organosulfurado que sirve como sal sódica de metanetiol. Se encuentra típicamente como un sólido blanco a blanco sucio, que es altamente soluble en agua debido a la presencia del ion sodio. Este compuesto se caracteriza por sus fuertes propiedades nucleofílicas, lo que lo hace útil en varias reacciones de síntesis orgánica, particularmente en la formación de tioéteres y otros compuestos que contienen azufre. Metanotiolato de sodio también es conocido por su capacidad para actuar como agente reductor y puede participar en reacciones que involucran electrófilos. Tiene un olor distintivo y penetrante que recuerda al repollo podrido, que es característico del metanetiol. Se requieren precauciones de seguridad al manipular este compuesto, ya que puede ser irritante para la piel, los ojos y el sistema respiratorio. Además, debe almacenarse en un lugar fresco y seco, alejado de sustancias incompatibles, para mantener su estabilidad y reactividad.
Fórmula:CH4S·Na
InChI:InChI=1S/CH4S.Na/c1-2;/h2H,1H3;
Clave InChI:InChIKey=XHXXWWGGXFUMAJ-UHFFFAOYSA-N
SMILES:CS.[Na]
Sinónimos:- (Methylsulfanyl)sodium
- Metanotiolato De Sodio
- Methanethiol, sodium salt (1:1)
- Methanethiolate de sodium
- Methyl mercaptan sodium salt
- Methylthiosodium
- Natriummethanthiolat
- Sodium Methanethiolate
- Sodium methanesulfenate
- Sodium methyl mercaptan
- Sodium methyl mercaptide
- Sodium methyl sulfide
- Sodium methylmercaptide
- Sodium methylthiolate
- Sodium thiomethoxide
- Sodium thiomethylate
- Sodium, (methylthio)-
- Thiomethoxide, Sodium
- Ver más sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Encontrado 11 productos.
Methyl Mercaptan Sodium Salt (ca. 15% in Water)
CAS:Fórmula:CH3NaSForma y color:Colorless to Light orange to Yellow clear liquidPeso molecular:70.08Sodium methanethiolate
CAS:Sodium methanethiolateFórmula:·CH3S·NaPureza:≥95%Forma y color: white to off-white crystalline powderPeso molecular:70.08929g/molSodium thiomethoxide
CAS:Fórmula:CH3NaSForma y color:White to yellow or brown powder or crystalsPeso molecular:70.09Sodium thiomethoxide solution
CAS:<p>Sodium thiomethoxide solution</p>Pureza:≥95%Forma y color:LiquidPeso molecular:70.08929g/molSodium Methanethiolate (~20% in Water)
CAS:Producto controlado<p>Applications 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.<br> E0<br>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),<br></p>Fórmula:CH3S·NaForma y color:ColourlessPeso molecular:70.09Sodium Methanethiolate (95%)
CAS:Producto controladoFórmula:CH3S·NaPureza:95%Forma y color:NeatPeso molecular:70.09Sodium methanethiolate
CAS:<p>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.</p>Fórmula:CH3NaSPureza:Min. 95%Forma y color:White PowderPeso molecular:70.09 g/mol3-Methyl-2-buten-1-thiol Preparation Kit
CAS:<p>Stability Readily Oxidized<br>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.<br>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),<br></p>Fórmula:MixtureVisitourWebsiteForma y color:Colourless To YellowPeso molecular:Mixture - Visit our WebsiteSodium methanethiolate - 15% aqueous solution
CAS:<p>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.</p>Fórmula:CH3NaSPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:70.09 g/molSodium Methanethiolate-13C
CAS:Producto controlado<p>Applications 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.<br>References Bergman, A. & Wachtmeister, Chemosphere, 7, 949 (1978); Suzuki, T.,et al.: Bioorg. Med. Chem. Lett., 14, 3313 (2004)<br></p>Fórmula:CH3NaSPureza:>90%Forma y color:NeatPeso molecular:71.082





