所有图片(2)
About This Item
线性分子式:
(O=)C5H7CO2CH3
CAS号:
分子量:
142.15
Beilstein:
971717
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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品質等級
化驗
95%
折射率
n20/D 1.456 (lit.)
bp
105 °C/19 mmHg (lit.)
密度
1.145 g/mL at 25 °C (lit.)
官能基
ester
ketone
儲存溫度
2-8°C
SMILES 字串
COC(=O)C1CCCC1=O
InChI
1S/C7H10O3/c1-10-7(9)5-3-2-4-6(5)8/h5H,2-4H2,1H3
InChI 密鑰
PZBBESSUKAHBHD-UHFFFAOYSA-N
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一般說明
对 2-氧代环戊烷甲酸甲酯与 Cr（III）在水溶液中的络合反应动力学已进行了研究。
應用
2-氧代环戊烷甲酸甲酯用于合成以下物质：
- 1,2-二取代的咪唑基甲基环戊醇衍生物
- 1-（4-溴丁基）-2-氧代环戊烷甲酸甲酯
- 1-（4-碘丁基）-2-氧代环戊烷甲酸甲酯
- 1-（3-溴丙基）-2-氧代环己烷甲酸乙酯
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
174.2 °F - closed cup
閃點（°C）
79 °C - closed cup
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Kinetics of monochelation of aqueous chromium (III) by methyl 2-oxocyclopentanecarboxylate.
Rojas A, et al.
Journal of Physical Organic Chemistry, 13(2), 97-104 (2000)
A Kato et al.
Chemical & pharmaceutical bulletin, 43(12), 2152-2158 (1995-12-01)
Two series of 1,2-disubstituted imidazolylmethylcyclopentanol derivatives (5a-d, 10a-d) were prepared by using easily available methyl 2-oxocyclopentanecarboxylate as the starting material. Evaluation of the aromatase inhibitory activities in vitro was performed. Their activities were compared with those of a steroidal aromatase
Nickel (I) Salen-Catalyzed Reduction of 1-Haloalkyl-2-oxocycloalkanecarboxylates Three-and Four-Carbon Ring Expansions.
Mubarak MS, et al.
Journal of the Electrochemical Society, 154(11), F205-F210 (2007)
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