121153-32-0

Basic information

• Product Name: Cyclohexane, 2-(methoxymethoxy)-4-methyl-1-(1-methylethyl)-, (1S,2R,4R)-
• CAS NO: 121153-32-0
• Molecular Formula: C12H24O2
• Molecular Weight: 200.321
• Mol File: 121153-32-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Cyclohexane, 2-(methoxymethoxy)-4-methyl-1-(1-methylethyl)-, (1S,2R,4R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexane, 2-(methoxymethoxy)-4-methyl-1-(1-methylethyl)-, (1S,2R,4R)-(121153-32-0)
• EPA Substance Registry System: Cyclohexane, 2-(methoxymethoxy)-4-methyl-1-(1-methylethyl)-, (1S,2R,4R)-(121153-32-0)

Safety Data

• Hazardous Substances Data: 121153-32-0(Hazardous Substances Data)

Upstream product

• 1201652-12-1 (-)-menthol-MOM-(d2) 
• 1201652-13-2 (-)-menthol-MOM-(d3) 
• 109-87-5 Dimethoxymethane 
• 2216-51-5 (-)-menthol 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 15356-70-4 menthol 
• 121153-31-9 menthyl phenylthiomethyl ether 
• 1201651-99-1 1-iodo-3-(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy)methyl)benzene 
• 1201651-97-9 1-((((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)oxy)methyl)-4-methylbenzene 
• 1201652-11-0 C₁₈H₂₆⁽²⁾H₂O 
• 351420-49-0 (1S,2R,4R)-2-(but-3-enyloxy)-1-isopropyl-4-methylcyclohexane 
• 1201652-09-6 C₁₄H₂₄⁽²⁾H₂O 
• 1201651-93-5 (3-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy)prop-1-ynyl)benzene 
• 1201652-08-5 C₁₉H₂₄⁽²⁾H₂O 
• 1201651-95-7 (1S,2R,4R)-1-isopropyl-4-methyl-2-((E)-undec-2-enyloxy)cyclohexane 
• 1201652-10-9 C₂₁H₃₈⁽²⁾H₂O 
• 1201652-00-7 1-bromo-3-(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy)methyl)benzene 
• 1201651-96-8 (1S,2R,4R)-2-((E)-6-chlorohex-2-enyloxy)-1-isopropyl-4-methylcyclohexane 
• 1201651-94-6 (3-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy)prop-1-ynyl)trimethylsilane 

Relevant articles and documents

Na-Y zeolite, an efficient catalyst for the methoxymethylation of alcohols

A variety of hydroxy compounds react with methoxymethyl chloride in the presence of catalytic amount of Na-Y zeolite to afford the corresponding methoxymethyl ethers (MOM ethers) in excellent yields.

An efficient protocol for the preparation of MOM ethers and their deprotection using zirconium(IV) chloride

An efficient protocol for the preparation of MOM ethers from alcohols and formaldehyde dimethyl acetal (DMFA) using ZrCl4 (10 mol %) at room temperature under solvent free conditions has been developed. Similarly, the same Lewis acid, ZrCl4 (50 mol %), in isopropanol at reflux was utilised for the deprotection of MOM ethers. An efficient protocol for the preparation of MOM ethers from alcohols and formaldehyde dimethyl acetal (DMFA) using ZrCl4 (10 mol %) at room temperature under solvent free conditions has been developed. Similarly, the same Lewis acid, ZrCl4 (50 mol %), in isopropanol at reflux was utilised for the deprotection of MOM ethers.