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Merck
CN

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
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Quality Level

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

SMILES string

CC(=O)C1CCCC1=O

InChI

1S/C7H10O2/c1-5(8)6-3-2-4-7(6)9/h6H,2-4H2,1H3

InChI key

OSWDNIFICGLKEE-UHFFFAOYSA-N

General description

2-Acetylcyclopentanone (2-ACP) is a β-dicarbonyl compound which undergoes keto-enol isomerization.

Application

2-Acetylcyclopentanone was used to evaluate the protective abilities of 2-ACP in a mouse model of acetaminophen (APAP) hepatotoxicity.


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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



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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



全球贸易项目编号

货号GTIN
179779-5G04061838754455
179779-100G04061836682835
179779-25G04061836682842