69435-89-8

Basic information

• Product Name: Trimethylsilyl=cyclohexanecarboxylate
• Synonyms: Cyclohexanecarboxylic acid trimethylsilyl ester;Trimethylsilyl=cyclohexanecarboxylate
• CAS NO: 69435-89-8
• Molecular Formula: C₁₀H₂₀O₂Si
• Molecular Weight: 0
• Mol File: 69435-89-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Trimethylsilyl=cyclohexanecarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: Trimethylsilyl=cyclohexanecarboxylate(69435-89-8)
• EPA Substance Registry System: Trimethylsilyl=cyclohexanecarboxylate(69435-89-8)

Safety Data

• Hazardous Substances Data: 69435-89-8(Hazardous Substances Data)

Upstream product

• 999-97-3 1,1,1,3,3,3-hexamethyl-disilazane 
• 98-89-5 Cyclohexanecarboxylic acid 
• 4630-82-4 methyl cyclohexylcarboxylate 
• 996-50-9 N,N-diethyl-1,1,1-trimethylsilanamine 
• 107-46-0 Hexamethyldisiloxane 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 76436-98-1 (Z)-1-cyclohexyl-1-(trimethylsilyloxy)-1-propene 
• 144808-60-6 cyclohexyl-3-methyl-4-methoxyphenyl ketone 
• 79320-50-6 <(3,5-di-tert-butyl-4-hydroxyphenyl)(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dienylidene)methyl>cyclohexane 
• 36263-61-3 1-(3-methoxyphenyl)cyclohexanecarboxylic acid 
• 79320-55-1 C₃₅H₅₁O₂ 
• 98-89-5 Cyclohexanecarboxylic acid 
• 7469-80-9 cyclohexyl 4-methoxyphenyl ketone 
• 70275-61-5 3-phenylpropyl cyclohexanecarboxylate 
• 119305-71-4 ((Z)-1-Cyclohexyl-3-phenyl-propenyloxy)-trimethyl-silane 

Relevant articles and documents

Synthesis of trimethylsilyl carboxylates by HMDS under solvent-free conditions

A broad set of structurally different carboxylic acids were transformed into their trimethylsilyl esters with HMDS in a practically completely solvent-free process, while a catalytic amount of iodine was required in some cases. The process has several advantages over the known methods: untreated reactants, air atmosphere, mild and neutral conditions, no evolution of hydrogen halide, no need of an additional base, low amount of waste, completely without chromatography, low consumption of energy, and operational simplicity.

1H and 13C ENDOR Investigations of Sterically Hindered Galvinoxyl Radicals

A variety of overcrowded novel galvinoxyl radicals have been synthesized.Steric requirements of bulky substituents have been studied by means of ESR, ENDOR, TRIPLE, and ENDOR-induced ESR spectroscopy.From 1H and 13C ENDOR measurements in nematic and smect