3-ethoxycyclopent-2-enone

Suppliers

Names

[ Name ]:
3-ethoxycyclopent-2-enone

[Synonym ]:
3-ethoxy-2-cyclopenten-1-one
3-ethoxy-2-cyclopentenone
EINECS 245-138-4
MFCD00042963
3-ethoxy-2-cyclopentene-1-one
3-Ethoxycyclopentenone
3-ethoxy-cyclopent-2-enone
2-Cyclopenten-1-one,3-ethoxy

Chemical & Physical Properties

[ Density]:
1.03g/cm3

[ Boiling Point ]:
229.7ºC at 760mmHg

[ Molecular Formula ]:
C₇H₁₀O₂

[ Molecular Weight ]:
126.15300

[ Flash Point ]:
101.8ºC

[ Exact Mass ]:
126.06800

[ PSA ]:
26.30000

[ LogP ]:
1.26970

[ Vapour Pressure ]:
0.0684mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.492(lit.)

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2914509090

Precursor & DownStream

Precursor

Cyclopentan-1,3-dion
Ethanol
2-Cyclopentene-1,4-dione

DownStream

3-tributylstannylcyclopent-2-en-1-one
2-BROMO-3-ETHOXYCYCLOPENT-2-ENONE
3-Amino-cyclopent-2-enone
3-ETHYLCYCLOPENTANONE
3-oxocyclopentene-1-carbonitrile
5-methyl-3-phenylcyclopent-2-en-1-one
3-ethylcyclopent-2-en-1-one
3-tert-butylcyclopent-2-en-1-one
2-Cyclopenten-1-one, 3-phenyl-
3-butylcyclopent-2-en-1-one

Customs

[ HS Code ]: 2914509090

[ Summary ]:
HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

Articles

Stereocontrolled synthesis of carbocyclic compounds with a quaternary carbon atom based on SN2' alkylation of γ,δ-epoxy-α,β-unsaturated ketones.

Org. Biomol. Chem. 10(28) , 5431-42, (2012)

We developed a new method for stereoselective construction of an all-carbon quaternary stereogenic center on a carbocyclic ring based on regio- and stereoselective S(N)2' alkylation reactions of γ,δ-e...

Manganese (III) acetate based tandem oxidation of various α and β-alkoxy α, β-unsaturated ketones. Tanyeli C, et al.

Tetrahedron 58(50) , 9983-9988, (2002)

Palladium-catalyzed rearrangements of 2-cyclopentenyloxypyrimidines in the preparation of pyrimidine carbonucleosides. Falck-Pedersen ML, et al.

Acta Chem. Scand. 47 , 72, (1993)

2-BROMO-3-ETHOXYCYCLOPENT-2-ENONE
3-phenylcyclohex-2-enone O-tosyloxime
3-IODOCYCLOHEX-2-ENONE
3-piperidinocyclohex-2-enone
3-BROMOCYCLOHEX-2-ENONE
3-methylcyclohex-2-enone oxime
N1-(3-ethylphenyl)-2-methylpropane-1,2-diamine
tert-butyl N-{2-[(2-aminoethyl)amino]ethyl}-N-methylcarbamate
2,2-difluoro-1-(1H-indol-3-yl)ethan-1-amine
3-Amino-4,4,5,5-tetradeuteriothiolan-2-one
N-Ethyl-2-fluoro-3-methylbenzene-1-sulfonamide
2-[(3-Methylfuran-2-yl)methyl]pyrrolidine
1,1-Difluoro-3-methyl-3-(methylamino)butan-2-ol
Methyl(3,4,4,4-tetrafluoro-2-methylbutan-2-yl)amine
5-Cyano-6-methylpyridine-3-sulfonamide
5-[(5-Bromo-2-chlorophenoxy)methyl]-1H-1,2,3,4-tetrazole

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