Nialamide

Application Cell-permeable NO donor releases nitric oxide spontaneously in a rate-controlled manner. Half-life in solution = 30 min.

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 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.

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

Synthetic chromogenic analog of sphingomyelin. Useful for measuring sphingomyelinase activity.

Application Reactant involved in synthesis of: Cyclic nitrogen compounds via intramolecular hydroamination Pentacyclic lycopodium alkaloid huperzine-Q Pyrrolidines Intermolecular C-H insertion reactions Reactant involved in intermolecular amination

Application Reactant involved in synthesis of: Cyclic nitrogen compounds via intramolecular hydroamination Pentacyclic lycopodium alkaloid huperzine-Q Pyrrolidines Intermolecular C-H insertion reactions Reactant involved in intermolecular amination

Application 2-Nitrobenzyl bromide was used for caging unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution . It can be used in the synthesis of ( R )- and ( S )-3-amino-3,4-dihydro-1 H -quinolin-2-one .

Application 2-Nitrobenzyl bromide was used for caging unprotected cysteine-containing or thiophosphorylated peptides in aqueous solution . It can be used in the synthesis of ( R )- and ( S )-3-amino-3,4-dihydro-1 H -quinolin-2-one .

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 3DPA2FBN is cyanoarene-based donor-acceptor photocatalyst developed by the Zeitler group. While this catalyst has a balanced redox profile, allowing for its use in a variety of transformations, it stands out as the most reducing