2085-26-9

Basic information

• Product Name: bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate
• Synonyms: bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate
• CAS NO: 2085-26-9
• Molecular Weight: 366.541
• Mol File: 2085-26-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate(CAS DataBase Reference)
• NIST Chemistry Reference: bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate(2085-26-9)
• EPA Substance Registry System: bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate(2085-26-9)

Safety Data

• Hazardous Substances Data: 2085-26-9(Hazardous Substances Data)

Upstream product

• 491-35-0 C₆H₄NCH₂CHCCH₂ 
• 70894-19-8 2-(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)oxy)-2-oxoacetic acid 
• 15356-70-4 menthol 
• 144-62-7 oxalic acid 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 81529-62-6 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-chloro-2-oxoacetate 
• 79-37-8 oxalyl dichloride 
• 2216-51-5 (-)-menthol 
• 298-12-4 Glyoxilic acid 
• 553-90-2 Dimethyl oxalate 
• 117530-32-2 methyl-((1R)-menthyl)-oxalate 

Downstream Products

• 20229-41-8 l-menthyl phenylglyoxylate 
• 636590-52-8 (1R,2S,5R)-menthyl 2-oxohexanoate 

Relevant articles and documents

Continuous flow synthesis of L-menthyl glyoxylate monohydrate: an important intermediate in the manufacture of antiretrovirals

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Microcapsules and uses thereof

The present invention relates to core-shell microcapsules comprising photolabile 2-oxoacetate pro-fragrance molecules capable of liberating an active molecule such as, for example, an aldehyde or ketone upon exposure to light. The present invention concerns also the use of said microcapsules in perfumery as well as the perfuming compositions or perfumed articles comprising the invention's microcapsules to provide a prolonged release of fragrant aldehydes and/or ketones.

Phase-vanishing reactions with ptfe (teflon) as a phase screen

Phase-vanishing reactions are triphasic reactions, which involve a reagent, a liquid perfluoroalkane, and a substrate. In a phase-vanishing reaction with PTFE tape as the phase screen instead of a liquid perfluoroalkane, there is no limitation related to the density of a phase and the denser phase can be in the top layer. The reactions were faster compared to traditional PV reactions, and it was possible to carry out sequential and tandem reactions and reactions under a reflux.