61548-81-0

Basic information

• Product Name: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate
• Synonyms: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate
• CAS NO: 61548-81-0
• Molecular Weight: 234.36
• Mol File: 61548-81-0.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate(61548-81-0)
• EPA Substance Registry System: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate(61548-81-0)

Safety Data

• Hazardous Substances Data: 61548-81-0(Hazardous Substances Data)

Usage

Description

(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate is a chemical compound with the molecular formula C10H20O3S. It is a cyclohexane derivative featuring a methyl and an isopropyl group, along with a methanesulfonate functional group that consists of a sulfur atom bonded to three oxygen atoms and a methyl group. (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate is known for its applications in organic synthesis and as a protecting group in chemical reactions.

Uses

Used in Organic Synthesis:
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate is utilized as a reagent for the formation of cyclohexylamine derivatives, which are important intermediates in the synthesis of various organic compounds.
Used as a Protecting Group in Organic Chemistry:
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate serves as an effective protecting group for alcohol and phenol functional groups during organic chemistry reactions, preventing unwanted side reactions and facilitating the synthesis of desired products.
Used in Pharmaceutical and Agrochemical Manufacturing:
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl methanesulfonate is also employed in the manufacturing processes of pharmaceuticals and agrochemicals, where its unique structural features contribute to the development of new and effective products.

Upstream product

• 2216-51-5 (-)-menthol 
• 124-63-0 methanesulfonyl chloride 
• 15356-70-4 menthol 

Downstream Products

• 134076-42-9 1-phenylselenenylneomenthane 
• 898543-45-8 2‐azido‐1‐isopropyl‐4‐methylcyclohexane 
• 1678-82-6 trans-1,4-menthane 
• 5113-93-9 (1R)-trans-p-menth-2-ene 
• 2623-23-6 L-menthyl acetate 
• 106137-43-3 (1S,2S,5R)-2-isopropyl-5-methylcyclohexyl formate 
• 107535-12-6 (1S,2S,4R)-2-azido-1-isopropyl-4-methylcyclohexane 
• 1207722-22-2 (1S,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexanecarbonyl Chloride 
• 70985-58-9 (1S,2S,5R)-2-isopropyl-5-methylcyclohexane-1-carboxylic acid 
• 80482-64-0 (1S,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxaldehyde 

Relevant articles and documents

Palladium(II)- and rhodium(I)-N-heterocyclic carbene complexes derived from menthol: Synthesis and characterisation

A carbene-Pd(II) complex and a carbene-Rh(I) complex, both derived from commercially available L-(-)-menthol, have been synthesised, characterised and their X-ray single-crystal structures determined.

Enantiopure encaged Verkade's superbases: Synthesis, chiroptical properties, and use as chiral derivatizing agent

Verkade's superbases, entrapped in the cavity of enantiopure hemicryptophane cages, have been synthesized with enantiomeric excess (ee) superior to 98%. Their absolute configuration has been determined by using electronic circular dichroism (ECD) spectros

Synthesis and in vitro antibacterial evaluation of novel 4-substituted 1-menthyl-1,2,3-triazoles

Menthyl 1,4-disubstituted 1,2,3-triazole derivatives of hydroxybenzaldehydes, phenols and bile acids were synthesized via click chemistry. The novel synthesized compounds were evaluated for their in vitro antibacterial activity against Enterococcus faeciu