Details
Quality Manufacturer Supply High Purity 99% ETHYL 3-(2-FURYL)PROPIONATE 10031-90-0 with Reasonable Price
- Molecular Formula: C9H12O3
- Molecular Weight: 168.192
- Vapor Pressure: 0.148mmHg at 25°C
- Refractive Index: n20/D 1.459(lit.)
- Boiling Point: 215.4 °C at 760 mmHg
- Flash Point: 92.3 °C
- PSA: 39.44000
- Density: 1.064 g/cm3
- LogP: 1.77530
ETHYL 3-(2-FURYL)PROPIONATE(Cas 10031-90-0) Usage
|
Preparation |
By direct esterification of the acid, which in turn is prepared by condensation of furfural with acetic anhydride and sodium acetate, followed by hydrogenation of the furacrylic acid |
|
Taste threshold values |
Taste characteristics at 15 ppm: pineapple, fruity, sweet, slightly spicy, tropical ripe and slightly jamy. |
InChI:InChI=1/C9H12O3/c1-2-11-9(10)6-5-8-4-3-7-12-8/h3-4,7H,2,5-6H2,1H3
10031-90-0 Relevant articles
Prostaglandins and congeners. XVIII. Synthesis of cyclopentenolone precursors to prostaglandins from 2,5-dihydro-2,5-dimethoxyfurans
Floyd
, p. 1641 - 1643 (1978)
-
One-Pot, Tandem Wittig Hydrogenation: Formal C(sp3)-C(sp3) Bond Formation with Extensive Scope
Devlin, Rory,Jones, David J.,Mcglacken, Gerard P.
, p. 5223 - 5228 (2020)
A one-pot, tandem Wittig hydrogenation o...
-
Matsuno,Han
, p. 155 (1937)
-
Preparation method of medium-and-long chain fatty carboxylic acid
-
Paragraph 0040-0044, (2019/04/04)
The application discloses a preparation ...
Structure-Odor Correlations in Homologous Series of Mercapto Furans and Mercapto Thiophenes Synthesized by Changing the Structural Motifs of the Key Coffee Odorant Furan-2-ylmethanethiol
Schoenauer, Sebastian,Schieberle, Peter
, p. 4189 - 4199 (2018/05/01)
Furan-2-ylmethanethiol (2-furfurylthiol;...
NOVEL COMPOUNDS
-
Page/Page column 96, (2008/12/06)
There is provided a compound of formula ...
10031-90-0 Process route
-
-
53282-12-5,53282-26-1
ethyl (E)-3-(2-furyl)prop-2-enoate
-
-
10031-90-0
ethyl 3-(furan-2-yl)propanoate
| Conditions | Yield |
|---|---|
|
With
hydrogen;
Wilkinson's catalist;
In
tetrahydrofuran;
at 45 ℃;
for 18h;
under 2585.81 Torr;
|
97%
|
|
With
hydrogen;
Lindlar's catalyst;
In
methanol;
for 8h;
|
82%
|
|
With
ammonium hydroxide; hydrogen;
nickel;
In
ethanol;
|
80%
|
|
With
ethanol; nickel;
at 110 - 120 ℃;
Hydrogenation;
|
|
|
With
carbon monoxide; hydrogen; benzene;
at 125 ℃;
under 19123.2 Torr;
Gegenwart von Octacarbonyldikobalt;
|
|
|
With
sodium amalgam; ethanol; acetic acid;
|
|
|
With
triethylsilane; silica gel;
Wilkinson's catalyst;
Yield given. Multistep reaction;
1.) benzene, room temperature, 8 h, 2.) petroleum ether, ethyl acetate;
|
-
-
64-17-5
ethanol
-
-
3-(2-furyl)acrylic acid p-tosylhydrazide
-
-
10031-90-0
ethyl 3-(furan-2-yl)propanoate
-
-
1858-86-2,59153-38-7,59203-02-0,112458-71-6
Ethyl p-toluenesulfinate
-
-
53282-12-5,53282-26-1
ethyl (E)-3-(2-furyl)prop-2-enoate
| Conditions | Yield |
|---|---|
|
With
toluene-4-sulfonic acid;
at 79 ℃;
for 60h;
|
19%
62% 21% |
10031-90-0 Upstream products
-
53282-12-5
ethyl (E)-3-(2-furyl)prop-2-enoate
-
64-17-5
ethanol
-
161890-25-1
ethyl 3-(3,4-dichlorophenylthio)-3-(2-furyl)propanoate
-
54536-91-3
3-(2-furyl)-propanoic acid chloride
10031-90-0 Downstream products
-
98334-58-8
3-[2]furyl-propionic acid hydrazide
-
106-30-9
ethyl heptanoate
-
14369-94-9
ethyl 4-oxoheptanoate
-
539-88-8
4-oxopentanoic acid ethyl ester
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