Difemetorex

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of rare and unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application 1,2-Diiodoethane can be used: To synthesize samarium(II) iodide-water complex (SmI 2 -H 2 O complex), a single-electron transfer reagent, to further synthesize 3-hydroxy carboxylic acids. To synthesize derivatives of regioselective

Application 1,2-Diiodoethane can be used: To synthesize samarium(II) iodide-water complex (SmI 2 -H 2 O complex), a single-electron transfer reagent, to further synthesize 3-hydroxy carboxylic acids. To synthesize derivatives of regioselective

1,3-Dithiane, a protected formaldehyde anion equivalent, serves as useful labeled synthon. Application 1,3-Dithiane was used as reagent for deoxygenation of sulfoxides to their corresponding sulfides.

1,3-Dithiane, a protected formaldehyde anion equivalent, serves as useful labeled synthon. Application 1,3-Dithiane was used as reagent for deoxygenation of sulfoxides to their corresponding sulfides.

Br(CH₂)₄Br CAS#: 110-52-1 F.W.: 215.93

1,4-Dithiane

Application Reagent for maintaining &#8722SH groups in the reduced state quantitatively reduces disulfides. Other Notes Cleavage of disulfide bonds in proteins Prevents oxidation of sulfhydryl-containing proteins during SDS-polyacrylamide gel

Application Reagent for maintaining &#8722SH groups in the reduced state quantitatively reduces disulfides. Other Notes Cleavage of disulfide bonds in proteins Prevents oxidation of sulfhydryl-containing proteins during SDS-polyacrylamide gel

Application Reagent for maintaining &#8722SH groups in the reduced state quantitatively reduces disulfides. reducing reagent

Application Reagent for maintaining &#8722SH groups in the reduced state quantitatively reduces disulfides. reducing reagent