116235-87-1

Usage

Chemical structure

A cyclohexane ring with two hydroxyl groups and three methyl groups attached at specific positions.

Common uses

Production of industrial and consumer products such as plastics, adhesives, and coatings.

Known for

Solvent properties.

Applications

Manufacturing of resins and polymers.

Additional uses

Reagent in organic synthesis and raw material for the production of other chemicals.

Safety precautions

Proper handling and safety measures should be taken to prevent potential hazards or health risks.

Upstream product

• 10276-21-8 isophorone oxide 
• 100507-98-0 trans-1,5,5-Trimethyl-3-(4-methylphenylsulfonyloxy)cyclohexanol 
• 100507-99-1 1,7,7-Trimethyl-2,4-dioxabicyclo<3.3.1>nonan-3-on 

Relevant academic research and scientific papers

Therapeutic and prophylactic agents for peptic ulcers

A therapeutic and prophylactic agent for peptic ulcers comprising as an effective ingredient a cyclohexane derivative represented by general formula (I): STR1 wherein A represents a group shown by formula, >CH2, STR2 wherein X represents ethynylene, vinylene or ethylene, Y represents oxo or a hydroxy group; R1, R3, R4 and R5 each represents a hydrogen atom or alkyl; R2 represents a hydrogen atom, alkyl or a group shown by --OR8 ; R6 represents a hydrogen atom, oxo or a group shown by --OR8 ; and R7 represents a hydrogen atom or a group shown by --OR8, wherein R8 represents a hydrogen atom or an organic residue.

Electroreductive Ring-Opening of α,β-Epoxy Carbonyl Compounds and Their Homologues through Recyclable Use of Diphenyl Diselenide or Diphenyl Ditelluride as a Mediator

A novel access to β-hydroxy carbonyl compounds from the corresponding α,β-epoxy compounds has been attained through the recyclable use of diphenyl diselenide or diphenyl ditelluride as an electroreduction mediator in a MeOH-NaClO4-(Pt) system. α,β-Epoxy ketones are converted to the corresponding aldols in the presence of malonic esters.Similarly, α,β-epoxy esters and nitriles can be reduced to the corresponding β-hydroxy compounds in the presence of acetic acid.

Syntheses and Conformational Properties of Stereoisomeric 1,3-Cyclohexanediol and 3-Aminocyclohexanol Derivatives. X-Ray Structure Analysis of trans-1,3-Dihydroxy-1,5,5-trimethylcyclohexane and c-3-Amino-r-1-hydroxy-1,5,5-trimethylcyclohexane

Solvomercuration of cyclohexenols 3 and 4 yields the respective cis/trans-diols 1a and pure trans-diol 2a.Via the monotosylates the analogous cis-diol cis-2a as well as the cis-amino alcohols cis-1b and cis-2b are prepared diastereomerically pure in good