5-ETHOXY-5H-FURAN-2-ONE supplier

Name
5-ETHOXY-5H-FURAN-2-ONE
EINECS 428-330-4
CAS No. 2833-30-9
Article Data19
CAS DataBase
Density 1.13 g/cm³
Solubility
Melting Point
Formula C₆H₈O₃
Boiling Point 262.8 °C at 760 mmHg
Molecular Weight 128.128
Flash Point 104.3 °C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms Crotonicacid, 4-ethoxy-4-hydroxy-, g-lactone (6CI,7CI);5-Ethoxy-2(5H)-furanone;5-Ethoxy-2,5-dihydro-2-furanone;b-Formylacrylic acid pseudoethyl ester;
PSA 35.53000
LogP 0.46200

Synthetic route

: 98-01-1
furfural

: 64-17-5
ethanol

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
With Eosin Y Irradiation;	60%
With Eosin Y; oxygen Irradiation;	53%
With oxygen in Gegenwart von Eosin und Vanadium(V)-oxid unter Bestrahlung mit Gluehlampenlicht;
With dihydrogen peroxide; vanadia 1) H2O, 50-55 deg C, 3 h, 2) benzene, reflux; Yield given. Multistep reaction;

: 6824-18-6
2,3,7-trioxa-bicyclo-<2.2.1>-hept-5-ene

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 82140-94-1, 94739-84-1
3,4-epoxy-butyrolactone

Conditions

Conditions	Yield
In chloroform -20 deg C, then 20 deg C, 1 h;	A n/a B 15% C n/a

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 5809-07-4
2-ethoxyfuran

B: 14032-66-7
5-hydroxy-2-(5H)-furanone

C: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A n/a B 40 % Chromat. C 12 % Chromat. D 12%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 2960-66-9
4-oxo-but-2-enoic acid ethyl ester

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: trans-2-hydroxy-5-ethoxy-2,5-dihydrofuran

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: cis-2-hydroxy-5-ethoxy-2,5-dihydrofuran

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: cis-2,5-diethoxy-2,5-dihydrofuran

: trans-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C 12% D 5%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: cis-2,5-diethoxy-2,5-dihydrofuran

D: 123-25-1
succinic acid diethyl ester

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C 12% D 1%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 4437-06-3
trans-β-formylacrylic acid

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 497-23-4
2-buten-4-olide

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C 2% D 12%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 87891-64-3
cis-2,5-dihydroxy-2,5-dihydrofuran

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 110-16-7
maleic acid

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given. Title compound not separated from byproducts;	A 40 % Chromat. B 12 % Chromat. C 2% D 12%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 110-17-8
(2E)-but-2-enedioic acid

D: cis-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given. Title compound not separated from byproducts;	A 40 % Chromat. B 12 % Chromat. C n/a D 12%

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: cis-2,5-diethoxy-2,5-dihydrofuran

: trans-2,5-diethoxy-2,5-dihydrofuran

Conditions

Conditions	Yield
With oxovanadium(IV) sulfate; ethanol; dihydrogen peroxide at 20℃; for 6h; Further byproducts given;	A 40 % Chromat. B 10% C 12% D 5%

...Expand

: 110-00-9
furan

: 64-17-5
ethanol

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
With oxygen in Gegenwart von Eosin;

: 110-00-9
furan

: 64-17-5
ethanol

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
With oxygen at 20℃;

...Expand

: 110-00-9
furan

A: 14032-66-7
5-hydroxy-2-(5H)-furanone

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
With oxygen In ethanol at 20℃; Irradiation;

: 14032-66-7
5-hydroxy-2-(5H)-furanone

: 64-17-5
ethanol

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
In chloroform at 70℃; Yield given;

: 61550-02-5
(furan-2-yloxy)-trimethylsilane

: 64-17-5
ethanol

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Conditions

Conditions	Yield
With iodosylbenzene; boron trifluoride diethyl etherate 1.) ethanol, 0 deg C, CH2Cl2; 2.) r.t.,overnight; Yield given. Multistep reaction;

: 5663-62-7
N-(furan-2-ylmethyl)acetamide

: 64-17-5
ethanol

oxygen: oxygen

A: 60-35-5
acetamide

B: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

C: 3852-14-0
N,N-methylenediacetamide

Conditions

Conditions	Yield
photosensibilisierte Reaktion;

...Expand

: 98-01-1
furfural

oxygen: oxygen

A: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

B: 109-94-4
formic acid ethyl ester

Conditions

Conditions	Yield
photosensibilisierte Reaktion;

...Expand

: 98-01-1
furfural

: 64-17-5
ethanol

A: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

B: 497-23-4
2-buten-4-olide

C: 623-91-6
diethyl Fumarate

D: 141-05-9
Diethyl maleate

Conditions

Conditions	Yield
Stage #1: furfural With vanadyl sulfate trihydrate; ethanol; dihydrogen peroxide at 60℃; Stage #2: ethanol With benzenesulfonic acid In chloroform Heating;

...Expand

: 3-bromo-5-ethoxyfuran-2(5H)-one

A: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

B: C6H7BrO3

C: C6H7BrO3

Conditions

Conditions	Yield
With OPR3; NADH In aq. buffer at 30℃; pH=7.5; Enzymatic reaction;	A n/a B n/a C n/a

...Expand

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 610-15-1
2-nitrobenzamide

: 2-Nitro-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	85%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 55-21-0
benzamide

: 62668-57-9
5-Benzoylamino-Δ3-oxolin-2-on

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	85%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 32978-38-4
4-bromo-5-ethoxyfuran-2(5H)-one

Conditions

Conditions	Yield
With bromine In tetrachloromethane at 0 - 20℃; for 3.5h;	82%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 7440-18-8
ruthenium

: 32978-38-4
4-bromo-5-ethoxyfuran-2(5H)-one

Conditions

Conditions	Yield
With bromine In tetrachloromethane	82%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 3424-93-9
4-methoxyphenylacetamide

: 4-Methoxy-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	80%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 57-13-6
urea

: (5-Oxo-2,5-dihydro-furan-2-yl)-urea

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	80%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 619-80-7
4-nitrobenzamide

: 4-Nitro-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	80%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 619-56-7
4-chlorobenzamide

: 4-Chloro-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	80%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 121-81-3
3,5-dinitrobenzamide

: 3,5-Dinitro-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	75%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 98604-39-8
3,4-dinitro-benzoic acid amide

: 3,4-Dinitro-N-(5-oxo-2,5-dihydro-furan-2-yl)-benzamide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	75%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 4648-54-8
trimethylsilylazide

: 6674-22-2
1,8-diazabicyclo[5.4.0]undec-7-ene

: 4-azido-5-ethoxy-dihydrofuran-2-one

Conditions

Conditions	Yield
With acetic acid In dichloromethane	73%

...Expand

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 96-41-3
Cyclopentanol

: (4S,5R)-5-ethoxy-4-(1-hydroxycyclopentyl)dihydrofuran-2(3H)-one

Conditions

Conditions	Yield
With bis(p-methoxyphenyl)methanone UV-irradiation;	73%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 80-62-6
methacrylic acid methyl ester

Copolymer, molecular weight 4000 amu, monomeric units - butenolide and vinyl compound - ratio in product 5:95, intrinsic viscosity 0.023 dl/g: Copolymer, molecular weight 4000 amu, monomeric units - butenolide and vinyl compound - ratio in product 5:95, intrinsic viscosity 0.023 dl/g

Conditions

Conditions	Yield
With dibenzoyl peroxide at 80℃; for 4.5h; Polymerization;	68%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 2244-06-6
undecanamide

: Undecanoic acid (5-oxo-2,5-dihydro-furan-2-yl)-amide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	65%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 629-54-9
Palmitamide

: Hexadecanoic acid (5-oxo-2,5-dihydro-furan-2-yl)-amide

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h;	65%

: 292638-84-7
styrene

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

Copolymer, molecular weight 3990 amu, monomeric units - butenolide and vinyl compound - ratio in product 4:96, intrinsic viscosity 0.025 dl/g: Copolymer, molecular weight 3990 amu, monomeric units - butenolide and vinyl compound - ratio in product 4:96, intrinsic viscosity 0.025 dl/g

Conditions

Conditions	Yield
With dibenzoyl peroxide at 80℃; for 9h; Polymerization;	64%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 698-16-8
benzohydroximoyl chloride

: 113003-50-2
3-phenyl-4-oxo-6-ethoxy-3a,4,6,6a-tetrahydrofuro<3,4-d>-isoxazole

Conditions

Conditions	Yield
With triethylamine In diethyl ether Ambient temperature; overnight;	61%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 108-05-4
vinyl acetate

Copolymer, molecular weight 4570 amu, monomeric units - butenolide and vinyl compound - ratio in product 60:40, intrinsic viscosity 0.022 dl/g: Copolymer, molecular weight 4570 amu, monomeric units - butenolide and vinyl compound - ratio in product 60:40, intrinsic viscosity 0.022 dl/g

Conditions

Conditions	Yield
With dibenzoyl peroxide at 80℃; for 4.5h; Polymerization;	61%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 67-63-0
isopropyl alcohol

: (4S,5R)-5-ethoxy-4-(2-hydroxypropan-2-yl)-dihydrofuran-2(3H)-one

Conditions

Conditions	Yield
With bis(p-methoxyphenyl)methanone UV-irradiation;	60%
With bis(p-methoxyphenyl)methanone for 0.166667h; UV-irradiation; Continuous-flow microreactor; Inert atmosphere; diastereoselective reaction;	100 %Spectr.

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 433733-19-8
2-benzyl-buta-2,3-dienoic acid ethyl ester

: 5-ethoxy-4-[1-benzyl-1-(ethoxycarbonyl)ethynyl]dihydrofuran-2(3H)-one

Conditions

Conditions	Yield
With sodium benzenesulfonate In N,N-dimethyl-formamide at 20℃; for 24h;	60%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 28123-63-9
4-chlorobenzohydroximoyl chloride

: 113003-51-3
(3aS,6R,6aR)-3-(4-Chloro-phenyl)-6-ethoxy-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one

Conditions

Conditions	Yield
With triethylamine In diethyl ether Ambient temperature; overnight;	57%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 591-51-5
phenyllithium

A: 955-83-9
2,5-diphenylfuran

B: 85704-21-8
hydroxy-2 diphenyl-5,5 dihydro-2,5 furanne

Conditions

Conditions	Yield
With water 1) THF, -70 deg C, 2) -20 deg C; Yield given. Multistep reaction;	A n/a B 57%
With water 1) THF, -70 deg C, 2) -20 deg C; Yield given. Multistep reaction;	A 12% B n/a

...Expand

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 584-02-1
2-pentanol

: (4S,5R)-5-ethoxy-4-(3-hydroxypentan-3-yl)dihydrofuran-2(3H)-one

Conditions

Conditions	Yield
With bis(p-methoxyphenyl)methanone UV-irradiation;	57%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 109-72-8, 29786-93-4
n-butyllithium

A: 72636-53-4
2,5-di(n-butyl)furan

B: 85704-19-4
hydroxy-2 di-n-butyl-5,5 dihydro-2,5 furanne

Conditions

Conditions	Yield
With water 1) THF, -70 deg C, 2) -20 deg C; Yield given. Multistep reaction;	A n/a B 55%
With water 1) THF, -70 deg C, 2) -20 deg C; Yield given. Multistep reaction;	A 5% B n/a

...Expand

: 60-35-5
acetamide

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 16275-44-8
4-acetamido-4-hydroxy-2-butenoic acid γ-lactone

Conditions

Conditions	Yield
With hydrogenchloride at 80℃; for 0.0833333h; Product distribution; var. acylamides;	45%
With hydrogenchloride at 80℃; for 0.0833333h;	45%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 36288-37-6
N-hydroxy-4-methylbenzenecarboximidoyl chloride

: 113003-55-7
(3aS,6R,6aR)-6-Ethoxy-3-p-tolyl-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one

Conditions

Conditions	Yield
With triethylamine In diethyl ether Ambient temperature; overnight;	40%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 29203-59-6
3-chloro-N-hydroxybenzimidoyl chloride

: 113003-53-5
(3aR,6S,6aS)-3-(3-Chloro-phenyl)-6-ethoxy-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one

Conditions

Conditions	Yield
With triethylamine In diethyl ether Ambient temperature; overnight;	40%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 2904-61-2
anthracene-9-carbonitrile N-oxide

: 113003-56-8
(3aS,6R,6aR)-3-Anthracen-9-yl-6-ethoxy-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one

Conditions

Conditions	Yield
In benzene at 80℃; for 4h;	40%

: 2833-30-9
5-ethoxy-2,5-dihydrofuran-2-one

: 53945-98-5
N-hydroxyfuran-2-carbimidoyl chloride

: 113003-57-9
(3aR,6S,6aS)-6-Ethoxy-3-furan-2-yl-6,6a-dihydro-3aH-furo[3,4-d]isoxazol-4-one

Conditions

Conditions	Yield
With triethylamine In diethyl ether Ambient temperature; overnight;	40%

5-ETHOXY-5H-FURAN-2-ONE Specification

The 2(5H)-Furanone,5-ethoxy- is an organic compound with the formula C₆H₈O₃. The systematic name of this chemical is 5-Ethoxyfuran-2(5H)-one. With the CAS registry number 2833-30-9, it is also named as 5-Ethoxy-5H-furan-2-one. Besides, its molecular weight is 128.13.

Physical properties about 2(5H)-Furanone,5-ethoxy- are: (1)ACD/LogP: -0.99; (2)ACD/LogD (pH 5.5): -0.98; (3)ACD/LogD (pH 7.4): -0.98; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 6.94; (7)ACD/KOC (pH 7.4): 6.94; (8)#H bond acceptors: 3; (9)#Freely Rotating Bonds: 2; (10)Polar Surface Area: 35.53 Å²; (11)Index of Refraction: 1.465; (12)Molar Refractivity: 31.26 cm³; (13)Molar Volume: 112.9 cm³; (14)Polarizability: 12.39×10^-24 cm³; (15)Surface Tension: 33.7 dyne/cm; (16)Density: 1.13 g/cm³; (17)Flash Point: 104.3 °C; (18)Enthalpy of Vaporization: 50.06 kJ/mol; (19)Boiling Point: 262.8 °C at 760 mmHg; (20)Vapour Pressure: 0.0107 mmHg at 25 °C.

You can still convert the following datas into molecular structure:
(1)InChI: InChI=1/C6H8O3/c1-2-8-6-4-3-5(7)9-6/h3-4,6H,2H2,1H3
(2)InChIKey: NOZLVOMKFMVAKH-UHFFFAOYAG
(3)Std. InChI: InChI=1S/C6H8O3/c1-2-8-6-4-3-5(7)9-6/h3-4,6H,2H2,1H3
(4)Std. InChIKey: NOZLVOMKFMVAKH-UHFFFAOYSA-N

Product Name

5-ETHOXY-5H-FURAN-2-ONE

Synthetic route

5-ETHOXY-5H-FURAN-2-ONE Specification

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