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1-acetyl cyclopentene

Names

[ CAS No. ]:
16112-10-0

[ Name ]:
1-acetyl cyclopentene

[Synonym ]:
1-(1-Cyclopenten-1-yl)ethanone
1-Acetyl-1-cyclopentene
1-acetyl-cyclopent-1-ene
Ethanone, 1-(1-cyclopenten-1-yl)-
1-(cyclopen-1-enyl)ethanone
1-Acetylcyclopentene
1-(1-cyclopentenyl)-ethanone
1-(cyclopent-1-en-1-yl)ethanone
1-aceto-1-cyclopentene
1-cyclopenten-1-yl methyl ketone
MFCD00799464
1-cyclopent-1-enyl-ethanone
1-acetyl cyclopentene

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
178.9±19.0 °C at 760 mmHg

[ Molecular Formula ]:
C7H10O

[ Molecular Weight ]:
110.154

[ Flash Point ]:
60.5±16.5 °C

[ Exact Mass ]:
110.073166

[ PSA ]:
17.07000

[ LogP ]:
1.12

[ Vapour Pressure ]:
1.0±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.485

MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H226

[ RIDADR ]:
UN 1224 3/PG 3

[ HS Code ]:
2914299000

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2914299000

[ Summary ]:
2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

Articles

Asymmetric intermolecular boron Heck-type reactions via oxidative palladium(II) catalysis with chiral tridentate NHC-amidate-alkoxide ligands.

J. Org. Chem. 75(1) , 95-101, (2010)

Chiral dimeric tridentate NHC-amidate-alkoxide palladium(II) complexes, 3a and 3b, effected oxidative boron Heck-type reactions of aryl boronic acids with both acyclic and cyclic alkenes at room tempe...

Synthesis of steroidal D-ring fused pyrazolines: study of regiochemistry of addition.

Steroids 59(8) , 479-84, (1994)

The addition of diphenylnitrilimine and C-o-chlorodiphenylnitrilimine to 3 beta-hydroxyandrost-5,16-diene (3b) produced a 1/1 ratio of regioisomeric, 1,3-diaryl-2-pyrazolines (6a, 7a and 6b, 7b), wher...

An intramolecular allenic [2+ 2+ 1] cycloaddition. Brummond KM, et al.

J. Org. Chem. 63(9) , 6535-6545, (1998)


More Articles


Related Compounds

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