179779
2-乙酰基环戊酮
98%
别名:
α-Acetylcyclopentanone, 2-Acetyl-1-cyclopentanone
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关于此项目
线性分子式:
CH3COC5H7(=O)
化学文摘社编号:
分子量:
126.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
216-797-5
Beilstein/REAXYS Number:
1857601
MDL number:
Assay:
98%
Form:
liquid
产品名称
2-乙酰基环戊酮, 98%
InChI key
OSWDNIFICGLKEE-UHFFFAOYSA-N
InChI
1S/C7H10O2/c1-5(8)6-3-2-4-7(6)9/h6H,2-4H2,1H3
SMILES string
CC(=O)C1CCCC1=O
assay
98%
form
liquid
refractive index
n20/D 1.489 (lit.)
bp
72-75 °C/8 mmHg (lit.)
density
1.043 g/mL at 25 °C (lit.)
functional group
ketone
Quality Level
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Application
2-Acetylcyclopentanone was used to evaluate the protective abilities of 2-ACP in a mouse model of acetaminophen (APAP) hepatotoxicity.
General description
2-Acetylcyclopentanone (2-ACP) is a β-dicarbonyl compound which undergoes keto-enol isomerization.
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
161.6 °F
flash_point_c
72 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Sungnam Park et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(4), 799-805 (2011-02-09)
2-Acetylcyclopentanone (2-ACP), which is a β-dicarbonyl compound, undergoes keto-enol isomerization, and its enol tautomers are stabilized by a cyclic intramolecular hydrogen bond. 2-ACP (keto form) has symmetric and asymmetric vibrational modes of the two carbonyl groups at 1748 and 1715
Lihai Zhang et al.
The Journal of pharmacology and experimental therapeutics, 346(2), 259-269 (2013-06-14)
Our previous research showed that enolates formed from 1,3-dicarbonyl compounds, such as 2-acetylcyclopentanone (2-ACP), could provide protection in cell culture models from electrophile- or oxidative stress-induced toxicity. In the present study, we evaluated the protective abilities of 2-ACP in a
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