Antipsychotic thioxanthenes

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.

Application Reactant for: Rhodium-catalyzed asymmetric hydrogenation reactions Wittig reaction Wittig methylenation Preparation of N -(phenylmethyl)- cis -pyrrolidinediacetic acid esters via double aza-Michael addition reaction Stereoselective

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.

1-(3-Carboxyphenyl)-2-thiourea (CPTU) is a thiourea derivative containing electron donor atoms (N and S). It acts as a ligand and readily form complexes with Hg(II).

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.

2,3-Diaminophenol is an aromatic diamine and forms Pd(II) and Pt(II) complexes. 2,3-Diaminophenol reacts with 2,4-pentanedione to yield the corresponding benzo[ b ][1,4]diazepinium salts.

2,3-Diaminophenol is an aromatic diamine and forms Pd(II) and Pt(II) complexes. 2,3-Diaminophenol reacts with 2,4-pentanedione to yield the corresponding benzo[ b ][1,4]diazepinium salts.

2,3-Dibromobenzo[b]thiophene

2,4-Dinitrophenol is called as an uncoupler of oxidative phosphorylation, which can prevent adenosine triphosphate(ATP) synthesis, but it permits electron transfer to proceed. 2,4-Dinitrophenol is called as an uncoupler of oxidative

Application 2,4-Dinitrophenol (DNP) can be used: As a reactant for catalytic reduction reactions. To activate carboxylic acids by converting them into dinitrophenyl (DNP) esters.