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3-butyldihydrofuran-2(3H)-one

  • CasNo:19340-56-8

Product Description

Factory supply 3-butyldihydrofuran-2(3H)-one 19340-56-8 with sufficient stock and high standard

  • Molecular Formula:C8H14 O2
  • Molecular Weight:142.198
  • Vapor Pressure:0.0408mmHg at 25°C 
  • Melting Point:108-110 °C 
  • Boiling Point:239.1°Cat760mmHg 
  • Flash Point:91.9°C 
  • PSA:26.30000 
  • Density:0.968g/cm3 
  • LogP:1.73970 

3-butyldihydrofuran-2(3H)-one(Cas 19340-56-8) Usage

InChI:InChI=1/C8H14O2/c1-2-3-4-7-5-6-10-8(7)9/h7H,2-6H2,1H3

19340-56-8 Relevant articles

Titanium tetrachloride promoted reaction of silyl ketene acetals with epoxides: A new method for the synthesis of γ-butanolides

Maslak, Veselin,Matovi?, Radomir,Sai?i?, Radomir N.

, p. 5411 - 5413 (2002)

A new method for the synthesis of γ-buta...

Economical, Green, and Safe Route Towards Substituted Lactones by Anodic Generation of Oxycarbonyl Radicals

Petti, Alessia,Leech, Matthew C.,Garcia, Anthony D.,Goodall, Iain C. A.,Dobbs, Adrian P.,Lam, Kevin

, p. 16115 - 16118 (2019/11/05)

A new electrochemical methodology has be...

Synthesis of substituted 2,3-dihydro-1H-boroles by transmetalation of aluminacyclopent-2-enes with BF3 · Et2O

Khafizova,Khusainova,Tyumkina,Dzhemilev

, p. 761 - 766 (2012/11/07)

A procedure was developed for selective ...

Reaction of silyl ketene acetals with epoxides: A new method for the synthesis of γ-butanolides

Maslak, Veselin,Matovi?, Radomir,Sai?i?, Radomir N.

, p. 8957 - 8966 (2007/10/03)

Titanium tetrachloride promoted reaction...

19340-56-8 Process route

oxirane
75-21-8,99932-75-9

oxirane

<<(α-methoxy)hex-1-enyl>oxy>trimethylsilane
84393-11-3

<<(α-methoxy)hex-1-enyl>oxy>trimethylsilane

α-butyl-γ-butyrolactone
19340-56-8

α-butyl-γ-butyrolactone

Conditions
Conditions Yield
oxirane; <<(α-methoxy)hex-1-enyl>oxy>trimethylsilane; With titanium tetrachloride; In dichloromethane; at -60 - -20 ℃;
With toluene-4-sulfonic acid; In dichloromethane; at 20 ℃;
69%
oxirane; <<(α-methoxy)hex-1-enyl>oxy>trimethylsilane; With titanium tetrachloride; In hexane; dichloromethane; at -60 - 20 ℃;
With toluene-4-sulfonic acid; In hexane; dichloromethane; at 20 ℃; for 3h;
69%
oxirane
75-21-8,99932-75-9

oxirane

2,2,6,6-tetramethyl-4-pentylidene-3,5-dioxa-2,6-disilaheptane
126736-77-4

2,2,6,6-tetramethyl-4-pentylidene-3,5-dioxa-2,6-disilaheptane

α-butyl-γ-butyrolactone
19340-56-8

α-butyl-γ-butyrolactone

Conditions
Conditions Yield
oxirane; 2,2,6,6-tetramethyl-4-pentylidene-3,5-dioxa-2,6-disilaheptane; With titanium tetrachloride; In hexane; dichloromethane; at -60 - 20 ℃;
With toluene-4-sulfonic acid; In hexane; dichloromethane; at 20 ℃; for 3h;
80%

19340-56-8 Upstream products

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    75-21-8

    oxirane

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    55011-28-4

    4,5-dihydro-4,4-dimethyl-2-pentyloxazole

  • 96-48-0
    96-48-0

    4-butanolide

  • 542-69-8
    542-69-8

    1-iodo-butane

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