Consentement d'utilisation des Cookies

J'accepte. Notre site sauvegarde des traceurs textes (cookies) sur votre appareil afin de vous garantir de meilleurs contenus et à des fins de collectes statistiques.Vous pouvez désactiver l'usage des cookies en changeant les paramètres de votre navigateur. En poursuivant votre navigation sur notre site sans changer vos paramètres de navigateur vous nous accordez la permission de conserver des informations sur votre appareil.

24057-28-1 - Pyridinium p-toluenesulfonate, 98+% - PPTS - Pyridinium tosylate - A15708 - Alfa Aesar

A15708 Pyridinium p-toluenesulfonate, 98+%

Numéro de CAS
24057-28-1
Synonymes
PPTS
Pyridinium tosylate

Conditionnement Prix ($) Quantité Disponibilité
25g 50,00
100g 161,00
500g 675,00
Ajouter au panier Ajouter au devis en vrac Afficher l'article

Pyridinium p-toluenesulfonate, 98+%

MDL
MFCD00013108
EINECS
246-002-7

Propriétés chimiques

Formule
C12H13NO3S
Poids moleculaire
251.31
Point de fusion
116-120°
Sensibilité
Moisture Sensitive
Solubilité
Soluble in water (partly), ethanol, acetone, dichloromethane, chloroform, methanol and dimethyl sulfoxide.

Applications

Pyridinium p-Toluenesulfate is used in the synthesis of a subdomain of the cytochrome P450 BM3 enzyme, for use in screening systems for drug candidates. Efficient catalyst for preparing tetrahydropyranyl ethers.

Notes

Moisture Sensitive. Store in a tightly closed container. Store in a cool, dry, well-ventilated. Store protected from moisture.

Références bibliographiques

Masaaki Miyashita; Akira Yoshikoshi; Paul A. Grieco. Pyridinium p-toluenesulfonate. A mild and efficient catalyst for the tetrahydropyranylation of alcohols. J. Org. Chem. 1977, 42 (23), 3772-3774.

Takeshi Matsukawa, Yoshihiro Mineno; Toru Odani; Shuji Okadab; Tetsuo Taniuchic;Synthesis and terahertz-wave generation of mixed crystals composed of 1-methyl-4-{2-[4-(dimethylamino)phenyl]ethenyl}pyridinium p-toluenesulfonate and p-chlorobenzenesulfonate. Journal of Crystal Growth. 2007, 299 (22), 344-348.

Mild catalyst for the formation of THP derivatives of alcohols superior to p-toluenesulfonic acid, where acid-sensitive functionality is present. Similarly, the reagent has been used for deprotection of THP ethers in ethanol: J. Org. Chem., 42. 3772 (1977).

This application has been extended to other acetalization or trans-acetalization reactions, where more acidic conditions are undesirable: Synthesis, 724 (1979).

For use in cleavage of TBDMS protecting groups, see: J. Chem. Soc. Perkin 1, 169 (1993).

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H315-H319-H335

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P261-P280a-P305+P351+P338-P304+P340-P405-P501a

Avoid breathing dust/fume/gas/mist/vapours/spray. Wear protective gloves and eye/face protection. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Beilstein
3764305
Code tarifaire harmonisé
2933.39
TSCA
Yes

Recommandé

Consulté récemment

Produits chimiques

Sciences de la vie

Métaux et matériaux

Catalyseurs

Analytique et matériel de laboratoire