1214906-07-6

Basic information

• Product Name: (-)-menthol
• Synonyms: (-)-menthol
• CAS NO: 1214906-07-6
• Molecular Weight: 156.268
• Mol File: 1214906-07-6.mol

Chemical Properties

• CAS DataBase Reference: (-)-menthol(CAS DataBase Reference)
• NIST Chemistry Reference: (-)-menthol(1214906-07-6)
• EPA Substance Registry System: (-)-menthol(1214906-07-6)

Safety Data

• Hazardous Substances Data: 1214906-07-6(Hazardous Substances Data)

Upstream product

• 1214906-08-7 C₁₃H₂₈OSi 

Downstream Products

• 147027-09-6 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl (2R,5R)-5-(methylcarbonyloxy)-1,3-oxathiolane-2-carboxylate 
• 1214906-08-7 C₁₃H₂₈OSi 
• 89-80-5 p-menthan-2-one 

Relevant articles and documents

P-toluenesulfonyl chloride (p-TsCl)-catalyzed trimethylsilylation of hydroxyl groups using hexamethyldisilazane and their regeneration under mild conditions: The first example for catalytic application of p-toluenesulfonyl chloride

The first catalytic application of p-toluenesulfonyl chloride (p-TsCl) for the efficient and selective trimethylsilylation of various types of hydroxyl groups with hexamethyldisilazane (HMDS) in dichloromethane and desilylation of these compounds in water is reported. The reactions were carried out at room temperature and were found to proceed in good to excellent yields.

Magnetic nanoparticle-supported DABCO tribromide: A versatile nanocatalyst for the synthesis of quinazolinones and benzimidazoles and protection/deprotection of hydroxyl groups

1,4-Diazabicyclo[2.2.2]octane tribromide supported on magnetic Fe3O4 nanoparticles (MNPs-DABCO tribromide) as a novel heterogeneous tribromide type compound was found to be an efficient and reusable nanocatalyst for the one-pot synthesis of 2-arylquinazolin-4(3H)-ones and 2-aryl-1H-benzo[d]imidazoles through oxidative cyclization of aldehydes with 2-aminobenzamides and 1,2-phenylenediamine, respectively. Also, MNPs-DABCO tribromide catalyzed trimethylsilylation/tetrahydropyranylation and desilylation/depyranylation of a wide variety of alcohols and phenols through changing the solvent medium at room temperature.