Passa al contenuto
Merck
Tutte le immagini(2)

Documenti

241776

Sigma-Aldrich

Potassium thioacetate

98%

Sinonimo/i:

Ethanethioic acid potassium salt, Thioacetic acid potassium salt, Thiolacetic acid potassium salt

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali


About This Item

Formula condensata:
CH3COSK
Numero CAS:
Peso molecolare:
114.21
Beilstein:
4428862
Numero CE:
Numero MDL:
Codice UNSPSC:
12352302
ID PubChem:
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

Punto di fusione

173-176 °C (lit.)

Stringa SMILE

[K+].CC([S-])=O

InChI

1S/C2H4OS.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
AFNBMGLGYSGFEZ-UHFFFAOYSA-M

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Descrizione generale

Potassium thioacetate is a sulfur source in sulfuration reactions and is used as a reagent in nucleophilic substitution and vinylic substitution reactions.

Applicazioni

Palladium mediated coupling with aryl halides and triflates leading to S-arylthioacetates and derivatives.
Reagent in the preparation of thiols from halides.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

Subal Dey et al.
Inorganic chemistry, 57(10), 5939-5947 (2018-05-02)
Reduction of CO2 holds the key to solving two major challenges taunting the society-clean energy and clean environment. There is an urgent need for the development of efficient non-noble metal-based catalysts that can reduce CO2 selectively and efficiently. Unfortunately, activation
Yang Wang et al.
Polymers, 11(6) (2019-06-13)
Photodynamic therapy (PDT) as a non-aggressive therapy with fewer side effects has unique advantages over traditional treatments. However, PDT still has certain limitations in clinical applications, mainly because most photosensitizers utilized in PDT are hydrophobic compounds, which will self-aggregate in
Tetrahedron Letters, 48, 3033-3033 (2007)
Christina Wedemeyer-Exl et al.
Organic & biomolecular chemistry, 5(13), 2119-2128 (2007-06-22)
The thiol-dependent methylation of heptamethyl cob(II)yrinate 8r with methyl iodide and methyl tosylate was explored under a variety of conditions. The interaction of the heptamethyl cob(II)yrinate with a variety of thiols was monitored prior to the addition of the methylating
Ning Shangguan et al.
Journal of the American Chemical Society, 125(26), 7754-7755 (2003-06-26)
A new amide synthesis strategy based on a fundamental mechanistic revision of the reaction of thio acids and organic azides is presented. The data demonstrate that amines are not formed as intermediates in this reaction. Alternative mechanisms proceeding through a

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.