CAS 121359-48-6
:2-(TRIBUTYLSTANNYL)THIAZOLE
- 2-(Tributylstannyl)-1,3-thiazole
- 2-(Tri-n-butylstannyl)thiazole
- 2-(Tributylstannanyl)-1,3-Thiazole
2-(Tri-n-butylstannyl)thiazole, 96%
CAS :Used as reagent for arylation of thiazole by Stille cross-coupling. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU refer
Formule :C15H29NSSnDegré de pureté :96%Couleur et forme :LiquidMasse moléculaire :374.172-(tributylstannyl)-1,3-thiazole
CAS :Formule :C15H29NSSnDegré de pureté :95%Couleur et forme :LiquidMasse moléculaire :374.16352-(Tributylstannyl)-1,3-thiazole
CAS :2-(Tributylstannyl)-1,3-thiazoleFormule :C15H29NSSnDegré de pureté :95%Couleur et forme : colourless liquidMasse moléculaire :374.17g/mol2-(Tributylstannyl)-1,3-thiazole
CAS :Produit contrôlé2-(Tributylstannyl)-1,3-thiazole is a coumarin derivative that contains a thiazole group. It has been shown to be a potent antagonist of the vitamin B1 coenzyme, which is an essential cofactor for the synthesis of purines and pyrimidines in many organisms. 2-(Tributylstannyl)-1,3-thiazole has been shown to inhibit molecular modeling and crystalline structure studies. These studies have revealed that the compound inhibits enzymes by blocking nucleophilic attack on the nitrogen atoms at position 1 and 3 on the thiazole ring. 2-(Tributylstannyl)-1,3-thiazole also inhibits cancer cells by cross-coupling with DNA. This inhibition leads to cellular death and prevents cancer from spreading to other tissues in the body.
Degré de pureté :Min. 95%




