709-83-1

Basic information

• Product Name: 2H-Pyran, 2-(cyclohexyloxy)tetrahydro-
• CAS NO: 709-83-1
• Molecular Formula: C11H20O2
• Molecular Weight: 184.279
• Mol File: 709-83-1.mol
• Article Data: 104

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, 2-(cyclohexyloxy)tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, 2-(cyclohexyloxy)tetrahydro-(709-83-1)
• EPA Substance Registry System: 2H-Pyran, 2-(cyclohexyloxy)tetrahydro-(709-83-1)

Safety Data

• Hazardous Substances Data: 709-83-1(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 108-93-0 cyclohexanol 
• 142-68-7 TETRAHYDROPYRANE 
• 69161-61-1 2-(prop-2-en-1-yloxy)oxane 
• 94800-75-6 2-(2,4,6-Trimethyl-phenoxy)-tetrahydro-pyran 
• 96754-03-9 2-(phenylsulfonyl)tetrahydro-2H-pyran 
• 57713-24-3 2-((1S,2S)-2-Bromo-cyclohexyloxy)-tetrahydro-pyran 
• 122-97-4 3-Phenyl-1-propanol 

Downstream Products

• 1927-74-8 5-Cyclohexyloxy-1-pentanol 
• 2412-73-9 benzoic acid cyclohexyl ester 
• 766-05-2 cyclohexane carbonitrile 
• 19573-22-9 cyclohexyl azide 
• 100-64-1 cyclohexanone-oxime 
• 930-68-7 cyclohexenone 
• 65335-82-2 [dimethyl(phenyl)silyloxy]cyclohexane 
• 4203-45-6 2-allyl-tetrahydro-pyran 
• 1253279-24-1 C₁₆H₂₈O₃ 
• 3173-53-3 Cyclohexyl isocyanate 
• 953-91-3 cyclohexyl tosylate 
• 782-84-3 Cyclohexyl benzenesulphonate 
• 16156-56-2 cyclohexyl mesylate 
• 4351-54-6 cyclohexyl formate 

Relevant articles and documents

Copper-Catalyzed Oxidative Acetalization of Boronic Esters: An Umpolung Strategy for Cyclic Acetal Synthesis

A protocol for the acetalization of boronic esters is described. The reaction is catalyzed by copper, and the conditions proved to be mild and were amenable to a variety of functional groups. We expanded the Chan-Lam coupling to include C(sp3) nucleophiles and converted them into corresponding acetals. This method allows for the orthogonal acetalization of substrates with reactive, acid-sensitive functional groups.

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.

Selective tetrahydropyranylation of alcohols and phenols using titanium(IV) salophen trifluoromethanesulfonate as an efficient catalyst

Titanium(IV) salophen trifluoromethanesulfonate, [TiIV(salophen)(OSO2CF3)2], as a catalyst enables selective tetrahydropyranylation of alcohols and phenols with 3,4-dihydro-2H-pyran. Using this catalytic system, primary, secondary and tertiary alcohols, as well as phenols, were converted to their corresponding tetrahydropyranyl ethers in high yields and short reaction times at room temperature. Investigation of the chemoselectivity of this method showed discrimination between the activity of primary alcohols in the presence of secondary and tertiary alcohols and phenols. This heterogenized catalyst could be reused several times without loss of its catalytic activity. Copyright