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5-Methylfuran-2-propionaldehyde
  • Chemical Name: 5-Methylfuran-2-propionaldehyde
  • CAS No.: 34756-16-6

Good factory exports good 5-Methylfuran-2-propionaldehyde 34756-16-6

  • Molecular Formula: C8H10O2
  • Molecular Weight: 138.166
  • Vapor Pressure: 0.62mmHg at 25°C 
  • Refractive Index: 1.47 
  • Boiling Point: 187.8 °C at 760 mmHg 
  • Flash Point: 75.1 °C 
  • PSA: 30.21000 
  • Density: 1.022 g/cm3 
  • LogP: 1.71950 

5-Methylfuran-2-propionaldehyde(Cas 34756-16-6) Usage

InChI:InChI=1/C8H10O2/c1-7-4-5-8(10-7)3-2-6-9/h4-6H,2-3H2,1H3

34756-16-6 Relevant articles

Halogen Bond-Catalyzed Friedel?Crafts Reactions of Furans Using a 2,2’-Bipyridine-Based Catalyst

Zhang, Huimiao,Toy, Patrick H.

supporting information, p. 215 - 221 (2020/12/01)

A halogen bond donor based on a 2,2’-bip...

A New Approach for the Synthesis of Highly Substituted Aromatic Rings: The Alkyne-Mediated Approach

Parsons, Philip J.,Jones, Daniel R.,Padgham, Alex C.,Allen, Lewis A. T.,Penkett, Clive S.,Green, Robert A.,White, Andrew J. P.

supporting information, p. 3981 - 3984 (2016/03/16)

Pentasubstituted aromatic rings serve as...

Photooxygenation of azidoalkyl furans: Catalyst-free triazole and new endoperoxide rearrangement

Kazancioglu, Elif Akin,Kazancioglu, Mustafa Zahrittin,Fistikci, Meryem,Secen, Hasan,Altundas, Ramazan

supporting information, p. 4790 - 4793 (2013/10/08)

Photooxygenation of azidoalkyl furans ha...

Photooxidations of 2-(γ,ε-dihydroxyalkyl) furans in water: Synthesis of DE-bicycles of the pectenotoxins

Kouridaki, Antonia,Montagnon, Tamsyn,Tofi, Maria,Vassilikogiannakis, Georgios

supporting information; experimental part, p. 2374 - 2377 (2012/07/01)

Photooxygenations of 2-(γ,ε-dihydroxyalk...

34756-16-6 Process route

2-methylfuran
534-22-5

2-methylfuran

acrolein
107-02-8,25068-14-8

acrolein

3-(5-methylfuran-2-yl)propanal
34756-16-6

3-(5-methylfuran-2-yl)propanal

Conditions
Conditions Yield
gold(III) chloride; In acetonitrile; at 20 ℃;
94%
With acetic acid; hydroquinone; In water; at 130 ℃; for 0.5h; Microwave irradiation;
93%
With acetic acid; hydroquinone; In water; at 130 ℃; for 0.666667h;
90%
With acetic acid; at 80 ℃; for 10h;
85%
With N,N'-dimethyl-3,3'-diiodo-2,2'-bipyridinium bis(tetrafluoroborate); In acetonitrile; at 20 ℃; for 4h; Inert atmosphere;
80%
Product distribution; Var. α,β-unsaturated oxo compounds;
With water; acetic acid; at 100 ℃; for 2h; under 2250180 Torr;
60 % Chromat.
2-methylfuran
534-22-5

2-methylfuran

acrolein
107-02-8,25068-14-8

acrolein

2,2',2''-propane-1,1,3-triyltris(5-methylfuran)

2,2',2''-propane-1,1,3-triyltris(5-methylfuran)

3-(5-methylfuran-2-yl)propanal
34756-16-6

3-(5-methylfuran-2-yl)propanal

Conditions
Conditions Yield
gold(III) chloride; In acetonitrile; at 20 ℃; for 24h;
98%

34756-16-6 Upstream products

  • 534-22-5
    534-22-5

    2-methylfuran

  • 107-02-8
    107-02-8

    acrolein

  • 17162-95-7
    17162-95-7

    3-(5-methyl-2-furanyl)-1-propanol

  • 67-68-5
    67-68-5

    dimethyl sulfoxide

34756-16-6 Downstream products

  • 120759-22-0
    120759-22-0

    2-[2-(5-Methyl-furan-2-yl)-ethyl]-4,4-diphenyl-1,4-dihydro-2H-benzo[d][1,3]oxazine

  • 81730-30-5
    81730-30-5

    2,4,6-Tri-β-(5-methyl-2-furylethyl)-1,3,5-trithiacycloxehane

  • 88909-19-7
    88909-19-7

    Benzoic acid (S)-3-hydroxy-5-(5-methyl-furan-2-yl)-pentyl ester

  • 88909-22-2
    88909-22-2

    Benzoic acid (R)-3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-5-(5-methyl-furan-2-yl)-pentyl ester