Fructone

Base Information

  • PRODUCT:Fructone
  • CAS.:6413-10-1
  • MF:C8H14O4
  • Molecular Weight:174.197
  • Purity:99%

Product Details

CAS: 6413-10-1

MF: C8H14O4

Buy cost-effective 99% pure Fructone 6413-10-1 now

  • Molecular Formula:C8H14O4
  • Molecular Weight:174.197
  • Vapor Pressure:0.219mmHg at 25°C 
  • Refractive Index:1.428 
  • Boiling Point:207.989 °C at 760 mmHg 
  • Flash Point:80.775 °C 
  • PSA:44.76000 
  • Density:1.067 g/cm3  
  • LogP:0.70260 

Fructone(Cas 6413-10-1) Usage

Trade name

Fructone (IFF), Jasmaprunat (Symrise)

InChI:InChI=1/C8H14O4/c1-3-10-7(9)6-8(2)11-4-5-12-8/h3-6H2,1-2H3

6413-10-1 Relevant articles

Synthesis, activity and mechanism for double-ring conjugated enones

Chen, Guangying,Huang, Gangliang,Liu, Jian,Zhou, Shiyang

, (2021)

The relationship between TLR4 and inflam...

Efficient and straightforward preparation of a building block for (-)-teubrevin G synthesis via chemically diversed oriented synthesis

Velazquez, Daniel Garcia,Luque, Rafael

, p. 7004 - 7007 (2011)

A rapid and efficient methodology to hig...

Design, synthesis and anti-rheumatoid arthritis evaluation of double-ring conjugated enones

Zhou, Shiyang,Zou, Huiying,Huang, Gangliang,Chen, Guangying,Zhou, Xueming,Huang, Shuheng

, (2021/02/22)

Four series of double-ring conjugated en...

Preparation of pyridine derivatives from the corresponding 5-acetal-1-carbonyl compounds by acid promoted cyclization

Konno, Hiroyuki,Mihara, Hiromichi,Watanabe, Yuki

, p. 1314 - 1329 (2021/07/19)

The synthesis of four alkylpyridine deri...

Br?nsted acidic cellulose-PO3H: An efficient catalyst for the chemoselective synthesis of fructones and trans-esterification via condensation of acetoacetic esters with alcohols and diols

Naikwadi, Dhanaji R.,Singh, Amravati S.,Biradar, Ankush V.

, (2021/10/04)

Cellulose is the most abundant organic s...

6413-10-1 Process route

ethyl acetoacetate
141-97-9

ethyl acetoacetate

ethylene glycol
107-21-1

ethylene glycol

(2-methyl-[1,3]dioxolan-2-yl)-acetic acid
5735-97-7

(2-methyl-[1,3]dioxolan-2-yl)-acetic acid

fructone
6413-10-1

fructone

Conditions
Conditions Yield
β-1 zeolite; In toluene; at 145.85 ℃; for 1h; Further Variations:; Catalysts; Temperatures; Pressures; Product distribution;
91%
4%
ethyl acetoacetate
141-97-9

ethyl acetoacetate

ethylene glycol
107-21-1

ethylene glycol

fructone
6413-10-1

fructone

Conditions
Conditions Yield
With montmorillonite K-10; In benzene; for 6h; Heating;
98%
With toluene-4-sulfonic acid; In benzene; for 48h; Reflux;
98.6%
With Amberlyst15; In cyclohexane; Reagent/catalyst; Solvent; Reflux;
97%
With boron trifluoride diethyl etherate; In dichloromethane; at 25 ℃; for 48h;
96%
USY-3 zeolite; In toluene; at 145.85 ℃; for 1h;
96%
With toluene-4-sulfonic acid;
96%
With chitosan immobilized with 3-(3-vinylimidazolyl)propane-1-sulfonate and 12-phosphotungstic acid; In cyclohexane; at 80 ℃; for 2h; Time; Reflux; Dean-Stark;
96.2%
With toluene-4-sulfonic acid; In benzene; for 17h; Heating;
95%
With toluene-4-sulfonic acid; In benzene; for 24h; Heating;
93%
With toluene-4-sulfonic acid; In benzene; Heating;
92%
With toluene-4-sulfonic acid; In benzene; for 8h; Heating;
91%
With toluene-4-sulfonic acid; In toluene; Reflux;
91%
With polyaniline-sulfate salt; In toluene; for 1.5h; Heating;
90%
With toluene-4-sulfonic acid;
90%
With toluene-4-sulfonic acid; In benzene; for 8h; Heating;
90%
With toluene-4-sulfonic acid; In benzene; for 5h; Heating;
90%
With toluene-4-sulfonic acid; In benzene; for 20h; Reflux;
88%
With toluene-4-sulfonic acid; In benzene; for 24h; Dean-Stark; Reflux;
87%
With toluene-4-sulfonic acid; In benzene; for 8h; Heating;
86%
With toluene-4-sulfonic acid; In toluene; for 4h; Reflux;
83%
With toluene-4-sulfonic acid; In toluene; for 12h; Heating;
80%
With toluene-4-sulfonic acid; In benzene; Heating;
75%
With toluene-4-sulfonic acid; In benzene; for 20h; Heating;
73%
With toluene-4-sulfonic acid; In benzene; for 24h; Heating;
70%
With N,N,N-triethyl-N-butanesulfonic acid ammonium hydrogen sulfate; at 79.99 ℃; for 2h; Temperature; Concentration; Reagent/catalyst; Time;
61.6%
With toluene-4-sulfonic acid; In benzene; Heating;
58%
With toluene-4-sulfonic acid; In toluene; for 5h; Dean-Stark; Heating;
54%
With toluene-4-sulfonic acid;
With toluene-4-sulfonic acid; In benzene;
With toluene-4-sulfonic acid; In benzene; Heating;
With carbon-based acid prepared by carbonization of furaldehyde and 2-hydroxyethylsulfonic acid; In cyclohexane; for 2.5h; Reflux;
With tin(II) hydroxide chloride; In neat (no solvent); at 100 ℃; for 2h; under 760.051 Torr; Reagent/catalyst;
With toluene-4-sulfonic acid; In toluene;
With toluene-4-sulfonic acid; In benzene; for 20h; Reflux;
With toluene-4-sulfonic acid; In toluene; for 2h; Dean-Stark; Reflux;
With toluene-4-sulfonic acid; In benzene; for 48h; Reflux;
With acidic PO3H-functionalized cellulose; In neat (no solvent); at 120 ℃; for 6h; Reagent/catalyst; Solvent; chemoselective reaction; Green chemistry;

6413-10-1 Upstream products

  • 141-97-9
    141-97-9

    ethyl acetoacetate

  • 107-21-1
    107-21-1

    ethylene glycol

6413-10-1 Downstream products

  • 5754-32-5
    5754-32-5

    2-(2-methyl-1,3-dioxolan-2-yl)ethanol

  • 5735-97-7
    5735-97-7

    (2-methyl-[1,3]dioxolan-2-yl)-acetic acid

  • 18871-63-1
    18871-63-1

    3,3-ethylenedioxybutanal

  • 141-97-9
    141-97-9

    ethyl acetoacetate

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