24602-40-2

Basic information

• Product Name: 3-(Trimethylsilyl)-1H-pyrazole
• Synonyms: 3-(Trimethylsilyl)-1H-pyrazole
• CAS NO: 24602-40-2
• Molecular Formula: C₆H₁₂N₂Si
• Molecular Weight: 140.26
• Mol File: 24602-40-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-(Trimethylsilyl)-1H-pyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(Trimethylsilyl)-1H-pyrazole(24602-40-2)
• EPA Substance Registry System: 3-(Trimethylsilyl)-1H-pyrazole(24602-40-2)

Safety Data

• Hazardous Substances Data: 24602-40-2(Hazardous Substances Data)

Upstream product

• 1066-54-2 trimethylsilylacetylene 
• 18107-18-1 diazomethyl-trimethyl-silane 

Downstream Products

• 78347-42-9 1-pyrazole 
• 92524-98-6 trimethyl(1-methylpyrazol-3-yl)silane 
• 92525-27-4 5-<(E)-1,3-diphenyl-1-(trimethylsiloxy)-2-propenyl>-1-methylpyrazole 
• 92525-15-0 1-methyl-5--3-(trimethylsilyl)pyrazole 
• 92525-24-1 5-<<4-(dimethylamino)phenyl>-(trimethylsiloxy)methyl>-pyrazole 
• 92525-26-3 1-methyl-5-<(E)-3-phenyl-1-(trimethylsiloxy)-2-propenyl>-1-methylpyrazole 
• 92525-25-2 1-methyl-5-<1-phenyl-1-(trimethylsiloxy)ethyl>-pyrazole 
• 92525-23-0 5-<4-chlorophenyl-(trimethylsiloxy)methyl>-1-methylpyrazole 
• 92525-14-9 1-methyl-5--pyrazole 
• 92525-18-3 1-methyl-3-pyrazole 
• 92524-99-7 1-methyl-5-(trimethylsilyl)-1H-pyrazole 

Relevant articles and documents

MODULATORS OF CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR

This disclosure provides modulators of Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), pharmaceutical compositions containing at least one such modulator, methods of treatment of cystic fibrosis using such modulators and pharmaceutical composi

Direct Alkenylation of Allylbenzenes via Chelation-Assisted C-C Bond Cleavage

A novel method for direct transformation of allyl groups in allylbenzene derivatives to alkenyl groups via rhodium-catalyzed C-C bond cleavage is reported. The alkenylation with styrenes of allylbenzenes containing pyridyl and pyrazolyl groups as a directing group proceeded efficiently to give alkenylation products. We also developed a new protocol for transformation of an ortho-prenylated phenol to an aniline derivative.