Tetracycline trihydrate

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.

2,2,3,3-Tetramethylbutane

Application 2,2,3,3-Tetramethylsuccinonitrile can be used as a reactant to synthesize: 3,4-Dihydro-3 H -pyrrol-2-imines by reacting with aryl lithium species in the presence of TMSCl. Phenyl substituted metal-free fused tetraazachlorins by

2,3-Naphthalocyanine

Application 2,4,6-Tri- tert -butylpyridine was used in the synthesis of indole triflones .

Application Ligand used in the &#945 -arylation of nitriles with aryl bromides and chlorides, and in the Stille cross-coupling of aryl chlorides. Together with Pd 2 (dba) 3 (Catalog Number 328774) forms a highly efficient catalyst for one-pot

Application Ligand used in the &#945 -arylation of nitriles with aryl bromides and chlorides, and in the Stille cross-coupling of aryl chlorides. Together with Pd 2 (dba) 3 (Catalog Number 328774) forms a highly efficient catalyst for one-pot

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 Catalyst for: Intermolecular hydroacylation of cyclopropenes Crossed acyloin condensations Domino ring-opening redox amidation Knoevenagel condensation Claisen rearrangement Lewis acid- and N-heterocyclic carbene-catalyzed

Application Catalyst for: Intermolecular hydroacylation of cyclopropenes Crossed acyloin condensations Domino ring-opening redox amidation Knoevenagel condensation Claisen rearrangement Lewis acid- and N-heterocyclic carbene-catalyzed

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3-Methylenecyclobutanecarbonitrile