58506-22-2

Basic information

• Product Name: 4-(2-hydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol
• Synonyms: 1,2-cyclohexanediol, 4-(1-hydroxy-1-methylethyl)-1-methyl-
• CAS NO: 58506-22-2
• Molecular Formula: C₁₀H₂₀O₃
• Molecular Weight: 188.264
• Mol File: 58506-22-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 287.5°C at 760 mmHg
• Flash Point: 131.8°C
• Density: 1.133g/cm³
• Vapor Pressure: 0.000277mmHg at 25°C
• Refractive Index: 1.52
• CAS DataBase Reference: 4-(2-hydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2-hydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol(58506-22-2)
• EPA Substance Registry System: 4-(2-hydroxypropan-2-yl)-1-methylcyclohexane-1,2-diol(58506-22-2)

Safety Data

• Hazardous Substances Data: 58506-22-2(Hazardous Substances Data)

Upstream product

• 138-86-3 limonene. 
• 98-55-5 terpineol 
• 7664-93-9 sulfuric acid 
• 145105-47-1 4,4,8-trimethyl-2,3-dioxabicyclo<3.3.1>nonane-8-ol 
• 54145-81-2 1,2-epoxy-8-hydroxy-p-menthane 
• 80-26-2 terpinyl acetate 
• 7785-53-7 4R-α-terpineol 
• 99-49-0 Carvone 
• 91547-99-8 (1R,2S,4R)-1,2-epoxy-p-menthan-8-ol 
• 88494-86-4 (1S,2R,4R)1,2-epoxy-p-menthan-8-ol 
• 5989-27-5 D-limonene 

Downstream Products

• 99-87-6 4-methylisopropylbenzene 
• 13833-08-4 1-methyl-4-(1-methylethenyl)-cyclohexane-1,2-diol 
• 498-71-5 sobrerol 
• 38235-58-4 trans-sobrerol 
• 23733-68-8 p-menth-3-en-2-one 
• 35572-37-3 1,8-dibromo-p-menthan-2-one 
• 116-51-8 terpenylic acid 
• 93542-80-4 2-tosyloxy-1,8-p-menthanediol 
• 132515-31-2 1,2,8-triacetoxy-p-menthane 
• 4436-81-1 homoterpenylmethylketone 

Relevant articles and documents

Selective Isomerization via Transient Thermodynamic Control: Dynamic Epimerization of trans to cis Diols

Traditional approaches to stereoselective synthesis require high levels of enantio- and diastereocontrol in every step that forms a new stereocenter. Here, we report an alternative approach, in which the stereochemistry of organic substrates is selectivel

An effective procedure for the synthesis of acid-sensitive epoxides: Use of 1-methylimidazole as the additive on methyltrioxorhenium-catalyzed epoxidation of alkenes with hydrogen peroxide

An effective method for suppression of ring opening and rearrangement of acid-sensitive epoxides during methyltrioxorhenium(MTO)-catalyzed epoxidation of alkenes with H2O2 by using 1-methylimidazole as a co-additive has been found. The combined use of 3-methylpyrazole and 1-methylimidazole as the additives has been found to be an effective procedure that affords excellent yields of acid-sensitive epoxides for MTO-catalyzed epoxidation.

Insect Growth Regulators, 20. - Synthesis of Cyclic Analogues of Juvenile Hormone-III

The cyclic analogue rac-14b of JH-III and its 2Z isomer rac-14a were obtained by a multi-step synthesis starting from rac-α-terpineol.The Wadsworth-Emmons reaction was applied to the formation of the carbon chain and to the introduction of the ester funct