18290-96-5

Upstream product

• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 124-38-9 carbon dioxide 
• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 

Downstream Products

• 1453266-14-2 1-[methoxy(methyl)phenylsilyl]-3,5-dimethyl-1H-pyrazole 
• 1453266-16-4 1-[dichloro(phenyl)silyl]-3,5-dimethyl-1H-pyrazole 
• 67-51-6 3,5-dimethyl-1H-pyrazole 
• 18279-61-3 trimethylsilyl diethylcarbamate 
• 56935-79-6 4-(3,5-dimethyl-1H-pyrazol-1-yl)benzonitrile 
• 50476-17-0 bis-(3,5-dimethylpyrazolyl)methanone 
• 10199-62-9 N,3,5-Trimethyl-1-pyrazolcarboxamid 
• 107-46-0 Hexamethyldisiloxane 
• 28791-82-4 1,1'-methylenebis(3,5-dimethyl-1H-pyrazole) 
• 91282-78-9 Benzoic acid (3aR,4R,6aR)-6-(3,5-dimethyl-pyrazol-1-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester 
• 89824-87-3 3,5-dimethyl-1-(2,3,5-tri-O-benzyl-β-D-arabinofuranosyl)pyrazole 
• 49652-39-3 1-(chloroformyl)-3,5-dimethylpyrazole 
• 124853-74-3 C₁₁H₁₈N₂O₃Si 
• 67-64-1 acetone 

Relevant academic research and scientific papers

Unusual course of diazolees silylation and N-siloxycarbonylation

The N-siloxycarbonylation and transamination reactions were studied by an example of diazoles. We found that because of insufficient nucleophilicity of the nitrogen atoms in the first case only the sililylation process occurs, in the second case the low-boiling amine is replaced by the higher boiling one and the process is completed by the formation of O-silyluretans. Pleiades Publishing, Ltd., 2011.