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Merck
CN

213063

4-氟苯甲酰乙酸甲酯

95%

别名:

3-(4-氟苯基)-3-氧丙酸甲酯

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关于此项目

线性分子式:
FC6H4COCH2CO2CH3
化学文摘社编号:
分子量:
196.18
EC Number:
263-889-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
3050469
MDL number:
Assay:
95%
Form:
liquid
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InChI key

HGLVYXXPRSNKQN-UHFFFAOYSA-N

InChI

1S/C10H9FO3/c1-14-10(13)6-9(12)7-2-4-8(11)5-3-7/h2-5H,6H2,1H3

SMILES string

COC(=O)CC(=O)c1ccc(F)cc1

assay

95%

form

liquid

refractive index

n20/D 1.521 (lit.)

density

1.228 g/mL at 25 °C (lit.)

functional group

ester, fluoro, ketone

Application

Methyl 4-fluorobenzoylacetate was used in the synthesis of:
  • 3-amino-4-(-4-fluoro-phenyl)furazan
  • series of substituted coumarin derivatives, potential 5-lipoxygenase inhibitors

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

One-pot synthesis of 3-amino-4-aryl-and 3-amino-4-hetarylfurazans.
Sheremetev AB.
Russian Chemical Bulletin, 54(4), 1057-1059 (2005)
Erich L Grimm et al.
Bioorganic & medicinal chemistry letters, 16(9), 2528-2531 (2006-02-09)
Leukotriene biosynthesis inhibitors have potential as therapeutic agents for asthma and inflammatory diseases. A novel series of substituted coumarin derivatives has been synthesized and the structure-activity relationship was evaluated with respect to their ability to inhibit the formation of leukotrienes

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