29779-72-4

Basic information

• Product Name: Cyclohexanol, 1,2,2,6,6-pentamethyl-
• CAS NO: 29779-72-4
• Molecular Formula: C11H22O
• Molecular Weight: 170.295
• Mol File: 29779-72-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Cyclohexanol, 1,2,2,6,6-pentamethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanol, 1,2,2,6,6-pentamethyl-(29779-72-4)
• EPA Substance Registry System: Cyclohexanol, 1,2,2,6,6-pentamethyl-(29779-72-4)

Safety Data

• Hazardous Substances Data: 29779-72-4(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 60-29-7 diethyl ether 
• 1195-93-3 2,2,6,6-tetramethylcyclohexanone 
• 74-88-4 methyl iodide 
• 38227-87-1 2,2,6,6-tetramethylpiperidinyl-lithium 

Downstream Products

• 46141-02-0 N,1,2,2,6,6-Hexamethylcyclohexylamin 
• 29779-75-7 1,2,2,6,6-Pentamethylcyclohexylamin 
• 81374-89-2 2-(Chlormethylen)-1,1,3,3-tetramethylcyclohexan 
• 81374-91-6 1,1,3,3-bis(1',1',5',5'-tetramethylpentamethylene)allene 
• 83357-84-0 Bis(2,2,6,6-tetramethylcyclohexanthiocarbonyl)disulfid 
• 83357-83-9 (2,2,6,6-Tetramethylcyclohexancarbonyl)(2,2,6,6-tetramethylcyclohexanthiocarbonyl)disulfid 
• 83357-82-8 Bis(2,2,6,6-tetramethylcylohexancarbonyl)sulfid 
• 83357-68-0 2,2,6,6-Tetramethyl-cyclohexanmethanol 
• 54439-96-2 2,2,6,6-Tetramethylcyclohexancarbonylchlorid 
• 13377-52-1 2.2.6.6-Tetramethyl-cyclohexan-carbonsaeure-⁽¹⁾ 
• 54440-00-5 (2,2,6,6-tetramethylcyclohexylidene)methanethione 
• 81675-70-9 p-Tolyl-carbamic acid 1,2,2,6,6-pentamethyl-cyclohexyl ester 
• 29779-78-0 1,1,3,3-Tetramethyl-2-methylencyclohexan 
• 29779-74-6 N-(1,2,2,6,6-Pentamethyl-cyclohexyl)-formamide 

Relevant articles and documents

A Grignard-type phase-vanishing method: Generation of organomagnesium reagent and its subsequent addition to carbonyl compounds

Abstract A quadraphasic phase-vanishing system comprised of diethyl ether, magnesium, perfluoropolyether, and iodoalkane efficiently generated the corresponding Grignard reagents, which subsequently added to carbonyl compounds in the ether layer to afford alkylated alcohols in good yields.