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安全信息

E51309

Sigma-Aldrich

1-戊烯-3-酮

contains 0.1% BHT as stabilizer, 97%

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别名:
乙基乙烯基酮
线性分子式:
C2H5COCH=CH2
CAS号:
1629-58-9
分子量:
84.12
Beilstein:
1735857
MDL编号:
MFCD00009316
PubChem化学物质编号:
24894604
NACRES:
NA.22

质量水平

200

检测方案

97%

形式

liquid

包含

0.1% BHT as stabilizer

折射率

n20/D 1.419 (lit.)

bp

38 °C/60 mmHg (lit.)

密度

0.851 g/mL at 20 °C
0.845 g/mL at 25 °C (lit.)

储存温度

−20°C

SMILES字符串

CCC(=O)C=C

InChI

1S/C5H8O/c1-3-5(6)4-2/h3H,1,4H2,2H3

InChI key

JLIDVCMBCGBIEY-UHFFFAOYSA-N

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相关类别

应用

成环反应试剂。
1-Penten-3-one can be used as a reactant to synthesize:
  • Conjugated dienes via palladium-catalyzed Heck reaction with vinyl bromides.
  • β-Amino carbonyl derivatives via solvent-free aza-Michael addition reaction with aromatic amines in the presence of ionic liquid catalyst.
  • α-Exo-methylene group bearing β-amino carbonyl compounds via ion-supported triphenylphosphine catalyzed aza‐Morita‐Baylis-Hillman reaction with N-tosyl arylimines.

警示用语：

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

14.0 °F - closed cup

闪点(°C)

-10 °C - closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

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Yuvaraju N Balamraju et al.
Journal of the American Chemical Society, 126(37), 11522-11528 (2004-09-16)
Oxidative cleavage of arachidonate (C(20)) and linoleate (C(18)) phospholipids generates truncated C(8) or C(12) gamma-hydroxyalkenal phospholipids as well as C(5) or C(9) carboxyalkanoate phospholipids, which are abundant in atherosclerotic plaques. The gamma-hydroxyalkenals promote foam cell formation by scavenger receptor CD36-mediated
D L Morgan et al.
Inhalation toxicology, 13(8), 633-658 (2001-08-11)
The National Toxicology Program is conducting a chemical class study to investigate the structure-activity relationships for the toxicity of alpha,beta-unsaturated ketones. Ethyl vinyl ketone (EVK) was selected for study because it is a representative straight-chain aliphatic alpha,beta-unsaturated ketone with extensive
Yingju Xu et al.
The Journal of organic chemistry, 74(14), 5100-5103 (2009-06-03)
A general approach for the synthesis of 3,5-diarylcyclopentenones was developed. Key aspects of this approach are the intramolecular Friedel-Crafts-type cyclization of vinyl chlorides and subsequent Pd-catalyzed cross-coupling reactions. The requisite vinyl chloride-bearing arylacetic acid precursors are readily available by straightforward
J C Meillon et al.
Nucleosides, nucleotides & nucleic acids, 24(5-7), 695-699 (2005-10-27)
2-Methyl-2-cyclopentene-1-one was used as starting material in a novel route toward 2'-branchedcarbocyclic nucleosides. This methodology was efficiently adapted to the preparation of 4'-epicarbocycles. A series of this new class of molecules was synthesized as potential antiviral compounds.
Synlett, 51-51 (1991)
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