168106
2-氧代环戊烷羧酸甲酯
95%
别名:
2-甲氧羰基环戊酮, 环戊酮-2-羧酸甲酯
登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
(O=)C5H7CO2CH3
化学文摘社编号:
分子量:
142.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
233-962-7
Beilstein/REAXYS Number:
971717
MDL number:
产品名称
2-氧代环戊烷羧酸甲酯, 95%
InChI key
PZBBESSUKAHBHD-UHFFFAOYSA-N
InChI
1S/C7H10O3/c1-10-7(9)5-3-2-4-6(5)8/h5H,2-4H2,1H3
SMILES string
COC(=O)C1CCCC1=O
assay
95%
refractive index
n20/D 1.456 (lit.)
bp
105 °C/19 mmHg (lit.)
density
1.145 g/mL at 25 °C (lit.)
functional group
ester
ketone
storage temp.
2-8°C
Quality Level
正在寻找类似产品? 访问 产品对比指南
Application
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
General description
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。
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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
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)
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)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持