29770
环戊酮
ReagentPlus®, ≥99.0%
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线性分子式:
C5H8(=O)
化学文摘社编号:
分子量:
84.12
EC Number:
204-435-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
605573
MDL number:
product line
ReagentPlus®
assay
≥99.0%
impurities
≤0.5% water
refractive index
n20/D 1.437
bp
130-131 °C (lit.)
mp
−51 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
SMILES string
O=C1CCCC1
InChI
1S/C5H8O/c6-5-3-1-2-4-5/h1-4H2
InChI key
BGTOWKSIORTVQH-UHFFFAOYSA-N
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Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2
存储类别
3 - Flammable liquids
wgk
WGK 1
flash_point_f
86.0 °F - closed cup
flash_point_c
30 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
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Koangyong Hyun et al.
Scientific reports, 7(1), 3825-3825 (2017-06-21)
The solution plasma process (SPP), known as non-equilibrium cold plasma at atmospheric pressure and room temperature, was used to investigate the synthesis of nitrogen-carbon nasnosheets (NCNs). To verify the effect of elementary composition and structure of N-methyl-2-pyrrolidone (NMP), various precursors
Ring Puckering in Five-Membered Rings. III. The Microwave Spectrum, Dipole Moment, and Structure of Cyclopentanone.
Kim H and Gwinn WD.
J. Chem. Phys. , 51(5), 181519-181519 (1969)
Piotr Neumann et al.
Plant physiology, 160(3), 1251-1266 (2012-09-19)
In plants, oxylipins regulate developmental processes and defense responses. The first specific step in the biosynthesis of the cyclopentanone class of oxylipins is catalyzed by allene oxide cyclase (AOC) that forms cis(+)-12-oxo-phytodienoic acid. The moss Physcomitrella patens has two AOCs
Lin Du et al.
Journal of natural products, 75(10), 1819-1823 (2012-10-11)
An uncommon 2,5-diarylcyclopentenone compound, preussidone (1), and a new biphenyl compound, 1',5-dimethoxy-3,5'-dimethyl-2,3'-oxybiphenyl-1,2'-diol (4), together with two known biphenyl compounds, 5-methoxy-3,5'-dimethyl-2,3'-oxybiphenyl-1,1',2'-triol (2) and cyperin (3), were obtained from a Preussia typharum isolate that was procured using a panel of unconventional media
Detoxification without intoxication: herbicide safeners activate plant defense gene expression.
Dean E Riechers et al.
Plant physiology, 153(1), 3-13 (2010-03-20)
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