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2-(TETRAHYDROFURFURYLOXY)TETRAHYDROPYRAN

  • CAS No.: 710-14-5
  • Purity: 99%
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Cost-effective and customizable 2-(TETRAHYDROFURFURYLOXY)TETRAHYDROPYRAN 710-14-5 factory

  • Molecular Formula: C10H18 O3
  • Molecular Weight: 186.251
  • Vapor Pressure: 0.00376mmHg at 25°C 
  • Refractive Index: n20/D 1.461(lit.) 
  • Boiling Point: 235-238ºC 
  • Flash Point: 208 °F 
  • PSA: 27.69000 
  • Density: 1.03 g/mL at 25ºC(lit.) 
  • LogP: 1.70860 

2-(TETRAHYDROFURFURYLOXY)TETRAHYDROPYRAN(Cas 710-14-5) Usage

InChI:InChI=1/C10H18O3/c1-2-6-12-10(5-1)13-8-9-4-3-7-11-9/h9-10H,1-8H2/t9-,10+/m0/s1

710-14-5 Relevant articles

AI(OTf)3 - A highly efficient catalyst for the tetrahydropyranylation of alcohols under solvent-free conditions

Kamal, Ahmed,Naseer A Khan,Srikanth,Srinivasa Reddy

scheme or table, p. 1099 - 1104 (2009/03/11)

A simple and highly efficient method has...

Bronsted acidic ionic liquids: Fast, mild, and efficient catalysts for solvent-free tetrahydropyranylation of alcohols

Duan, Zhiying,Gu, Yanlong,Deng, Youquan

, p. 1939 - 1945 (2007/10/03)

Bronsted acidic ionic liquids as efficie...

A simple and efficient tetrahydropyranylation using N-bromosuccinamide

Das, Biswanath,Reddy, M. Ravinder,Ravindranath,Reddy, V. Saidi,Venkateshwarlu

, p. 1711 - 1712 (2007/10/03)

Tetrahydropyranylation of hydroxyl group...

Phosphorus pentoxide as an efficient catalyst for the tetrahydropyranylation of alcohols under solvent-free conditions

Eshghi, Hossein,Shafieyoon, Parvaneh

, p. 2149 - 2152 (2007/10/03)

A facile and efficient method for the pr...

710-14-5 Process route

Tetrahydrofurfuryl alcohol
97-99-4

Tetrahydrofurfuryl alcohol

3,4-dihydro-2<i>H</i>-pyran
110-87-2

3,4-dihydro-2H -pyran

tetrahydrofurfuryl tetrahydropyranyl ether
710-14-5

tetrahydrofurfuryl tetrahydropyranyl ether

Conditions
Conditions Yield
With zirconium(IV) chloride; In dichloromethane; for 3h;
99%
With Envirocat EPZG; at 0 - 5 ℃; for 1h;
98%
With 1-butyl-3-methylimidazolium hydrogen sulfate; at 20 ℃; for 0.166667h;
98%
With iron(II) sulfate; for 0.0583333h; Irradiation;
97%
With sulfated zirconia; In dichloromethane; for 0.5h; Ambient temperature;
90%
With Zr(O3PCH3)1.2(O3PC6H4SO3H)0.8; In dichloromethane; for 1h; Ambient temperature;
90%
N-Bromosuccinimide; In dichloromethane; at 20 ℃; for 1.25h;
86%
With aluminium(III) triflate; at 20 ℃; for 30h;
86%
H-Y zeolite; In hexane; for 4h; Heating;
85%
With calcium chloride; In dichloromethane; at 25 ℃; for 2h;
85%
With phosphorus pentaoxide; at 20 ℃; for 0.166667h;
85%
With phosphotungstic acid 44-hydrate; In dichloromethane; for 2h; Ambient temperature;
63%
With hydrogenchloride;
tetrahydrofurfuryl tetrahydropyranyl ether
710-14-5

tetrahydrofurfuryl tetrahydropyranyl ether

Conditions
Conditions Yield

710-14-5 Upstream products

  • 97-99-4
    97-99-4

    Tetrahydrofurfuryl alcohol

  • 110-87-2
    110-87-2

    3,4-dihydro-2H -pyran

710-14-5 Downstream products

  • 637-64-9
    637-64-9

    tetrahydrofurfuryl acetate

  • 97-99-4
    97-99-4

    Tetrahydrofurfuryl alcohol

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