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CAS No.: | 6270-56-0 |
---|---|
Name: | 2-(ETHOXYMETHYL)FURAN |
Article Data: | 27 |
Molecular Structure: | |
Formula: | C7H10O2 |
Molecular Weight: | 126.155 |
Synonyms: | 2-(Ethoxymethyl)furan;Ethyl furfuryl ether;Furfuryl ethyl ether;NSC 35558; |
EINECS: | 228-454-7 |
Density: | 0.986 g/cm3 |
Boiling Point: | 136.5 °C at 760 mmHg |
Flash Point: | 41.2 °C |
PSA: | 22.37000 |
LogP: | 1.81610 |
Conditions | Yield |
---|---|
With tin(IV) oxide at 200℃; for 20h; Temperature; Reagent/catalyst; | 95% |
With arenesulfonic acid and phenyl groups functionalized ethane bridged organosilica nanohybrid at 120℃; for 0.5h; Reagent/catalyst; Autoclave; | |
With Zr-mesoporous silica (SBA-15) at 100℃; for 5h; | |
With niobium pentoxide nanowires calcined at 100 ∘C at 100℃; under 6000.6 Torr; for 5h; |
(2-furyl)methyl alcohol
ethanol
A
2-(ethoxymethyl)furan
B
4,5,5-triethoxypentan-2-one
C
4-oxopentanoic acid ethyl ester
Conditions | Yield |
---|---|
at 110℃; for 2h; Temperature; Reagent/catalyst; Autoclave; Ionic liquid; | A n/a B n/a C 92% |
With hydrothermally treated graphene oxide (GO-HT) at 120℃; for 6h; Autoclave; | A 38.8% B 11.7% C 39.7% |
(2-furyl)methyl alcohol
ethanol
A
2-(ethoxymethyl)furan
B
4-oxopentanoic acid ethyl ester
Conditions | Yield |
---|---|
With sulfonic acid-functionalized MIL-101(Cr) at 140℃; for 2h; Temperature; Reagent/catalyst; Autoclave; | A n/a B 79.2% |
With hierarchical-HZ-5 at 99.84℃; for 4h; Catalytic behavior; Green chemistry; | A 26% B 73% |
With hierarchical-HZ-5 at 99.84℃; for 4h; Catalytic behavior; Green chemistry; | A 49% B 41% |
2-(diethoxymethyl)furan
A
furfural
B
2-(ethoxymethyl)furan
C
Ethyl 2-furoate
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane at 0℃; for 0.25h; | A 19% B 54% C 15% |
With boron trifluoride diethyl etherate In 1,2-dichloro-ethane at 0℃; for 0.25h; Mechanism; | A 19% B 54% C 15% |
monoaluminum phosphate at 150℃; Product distribution; other catalysts ( γ-alumina, γ-aluminium sulphate), other temperatures, other (substituted) furaldehyde acetals; |
(2-furyl)methyl alcohol
ethanol
A
2-(ethoxymethyl)furan
B
2-(diethoxymethyl)furan
C
4-oxopentanoic acid ethyl ester
Conditions | Yield |
---|---|
With silica-supported nickel phosphide at 180℃; under 750.075 Torr; for 3h; Temperature; Inert atmosphere; Autoclave; | A 53.7% B 7.4% C 35.3% |
(2-furyl)methyl alcohol
ethanol
A
2-(ethoxymethyl)furan
B
4,5,5-triethoxypentan-2-one
Conditions | Yield |
---|---|
With graphene oxide at 80℃; for 6h; Autoclave; | A 22.2% B 12.3% |
Conditions | Yield |
---|---|
With potassium hydroxide; diethyl ether at 75 - 80℃; |
Conditions | Yield |
---|---|
With potassium hydroxide; diethyl ether |
Conditions | Yield |
---|---|
With potassium hydroxide |
tri-n-butyl-tin hydride
2-(furan-2-yl)-1,3-oxathiolane
A
2-(ethoxymethyl)furan
B
C19H36O2SSn
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In benzene Product distribution; Heating; |
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The Furan, 2-(ethoxymethyl)-, with the CAS registry number of 6270-56-0, is also known as Ethyl furfuryl ether. Its EINECS registry number is 228-454-7. This chemical's molecular formula is C7H10O2 and molecular weight is 126.15. What's more, its IUPAC name is 2-(Ethoxymethyl)furan.
Physical properties about Furan, 2-(ethoxymethyl)- are: (1)ACD/LogP: 1.65; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.65; (4)ACD/LogD (pH 7.4): 1.65; (5)ACD/BCF (pH 5.5): 10.56; (6)ACD/BCF (pH 7.4): 10.56; (7)ACD/KOC (pH 5.5): 188.15; (8)ACD/KOC (pH 7.4): 188.15; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 22.37 Å2; (13)Index of Refraction: 1.451; (14)Molar Refractivity: 34.47 cm3; (15)Molar Volume: 127.9 cm3; (16)Polarizability: 13.66×10-24 cm3; (17)Surface Tension: 29.1 dyne/cm; (18)Density: 0.986 g/cm3; (19)Flash Point: 41.2 °C; (20)Enthalpy of Vaporization: 35.85 kJ/mol; (21)Boiling Point: 136.5 °C at 760 mmHg; (22)Vapour Pressure: 9.11 mmHg at 25 °C.
Preparation: this chemical is prepared by Furfural-diethylacetal. The reaction needs reagent BF3O(C2H5)2 and solvent 1, 2-Dichloro-ethane. The reaction time is 15 minutes with reaction temperature of 0 °C. The yield is about 54 %.
Uses: it is used to produce other chemicals. For example, it is used to produce 5-Ethoxymethyl-furfuryl alcohol. This reaction needs reagent Acetic acid. Other condition of this reaction is reaction time of 3 hours at 70-80 °C. The yield is about 46 %.
You can still convert the following datas into molecular structure:
(1) SMILES: O(CC)Cc1occc1
(2) InChI: InChI=1/C7H10O2/c1-2-8-6-7-4-3-5-9-7/h3-5H,2,6H2,1H3
(3) InChIKey: BHGBNDNKYPEAAT-UHFFFAOYAB