3-ethoxycyclopent-2-enone

Suppliers

Names

[ CAS No. ]:
22627-70-9

[ 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

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)


More Articles


Related Compounds

  • 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
  • 4-methoxy-N,N-dimethyl-5-(2-methylbut-3-yn-2-yl)-1,3-thiazol-2-amine
  • 3-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylpentanoyl]-3-azabicyclo[3.1.0]hexane-1-carboxylic acid
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 3-{[(2-Bromo-5-fluorophenyl)methyl]amino}-1lambda6-thietane-1,1-dione
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • CID 169552968