136375-73-0

Basic information

• Product Name: [[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]methyl]benzene
• Synonyms: [[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]methyl]benzene
• CAS NO: 136375-73-0
• Molecular Weight: 246.393
• Mol File: 136375-73-0.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: [[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]methyl]benzene(136375-73-0)
• EPA Substance Registry System: [[[(1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl]oxy]methyl]benzene(136375-73-0)

Safety Data

• Hazardous Substances Data: 136375-73-0(Hazardous Substances Data)

Upstream product

• 2216-51-5 (-)-menthol 
• 100-39-0 benzyl bromide 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 882980-43-0 2-benzyloxy-1-methylpyridinium triflate 
• 180477-54-7 (1S,2R,4R)-1-isopropyl-4-methyl-2-(3-methylbut-2-en-1-yloxy)cyclohexane 
• 121153-32-0 (-)-menthol-MOM 
• 7285-83-8 2,4,6-tris(benzyloxy)-1,3,5-triazine 
• 100-51-6 benzyl alcohol 
• 18419-38-0 (-)-menthol trimethylsilyl ether 
• 100-52-7 benzaldehyde 
• 1078-58-6 diphenylzinc 
• 26127-08-2 (1R,2S,5R)-1-(chloromethoxy)-2-isopropyl-5-methylcyclohexane 
• 1327239-34-8 N-(((1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy)methoxy)-N-methylacetamide 
• 753488-83-4 (1S,2R,4R)-2-(2,3-dimethylbut-2-en-1-yloxy)-1-isopropyl-4-methylcyclohexane 

Downstream Products

• 2216-51-5 (-)-menthol 
• 440122-04-3 α-azidobenzyl (-)-menthyl ether 
• 2623-23-6 L-menthyl acetate 
• 65-85-0 benzoic acid 
• 59632-78-9 (((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)oxy)dimethyl(phenyl)silane 
• 40940-58-7 (1S,2R,4R)-2-(allyloxy)-1-isopropyl-4-methylcyclohexane 
• 612-33-9 L-menthyl benzoate 
• 136289-27-5 (R)-1-[(R)-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-phenyl-methyl]-1,2-dihydro-naphthalene-1,4-dicarbonitrile 
• 136289-27-5 (R)-1-[(S)-((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-phenyl-methyl]-1,2-dihydro-naphthalene-1,4-dicarbonitrile 

Relevant articles and documents

Development of triazine-based benzylating reagents possessing T-butyl group on the triazine core: Thermally controllable reagents for the initiation of reaction

Benzylating reagents, 4-(4,6-di-t-butyl-1,3,5-triazin-2-yl)-4-benzylmorpholinium triflate, and related derivatives have been developed. The reagents release benzyl triflate as a benzyl cation equivalent upon heating the solution to 40°C under neutral conditions. The O-benzylation of alcohols using a stoichiometric amount of these reagents afforded corresponding benzyl ethers in good to high yields. This was due to the presence of a bulky t-butyl group on the triazine ring of these reagents that prevents the consumption of benzyl triflate via a side reaction with a morpholinotriazine derivative.

TRIAZINE DIONE COMPOUND

PROBLEM TO BE SOLVED: To provide a novel triazine dione compound useful as an alkylating agent for a nucleophilic compound. SOLUTION: This invention relates to a compound represented by formula (I) [where each symbol is as defined in the specification] and an alkylating agent comprising the compound, and a method for alkylating a nucleophilic compound using the alkylating agent. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT

Triazine compound

PROBLEM TO BE SOLVED: To provide a novel triazine compound useful as an agent for arylmethylating a nucleophilic compound. SOLUTION: This invention relates to a compound represented by formula (I) [where each symbol is as defined in the specification], an