410616
4-苄氧基-2(1H)-吡啶酮
99%
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关于此项目
经验公式（希尔记法）:
C12H11NO2
化学文摘社编号:
分子量:
201.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
InChI
1S/C12H11NO2/c14-12-8-11(6-7-13-12)15-9-10-4-2-1-3-5-10/h1-8H,9H2,(H,13,14)
SMILES string
O=C1NC=CC(OCc2ccccc2)=C1
InChI key
DOVNUEPFPBWTSV-UHFFFAOYSA-N
assay
99%
form
solid
mp
201-203 °C (lit.)
General description
N-alkylation of 4-benzyloxy-2(1H)-pyridone with the corresponding benzyl halides has been reported.
Application
在温和无水条件下吡啶氮可与 n-Bu4I 和 KOBu-t 发生烷基化反应。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Tetrahedron Letters, 46, 7917-7917 (2005)
Suresh K Tipparaju et al.
Bioorganic & medicinal chemistry letters, 18(12), 3565-3569 (2008-05-24)
Enoyl-ACP reductase (ENR), the product of the FabI gene, from Bacillus anthracis (BaENR) is responsible for catalyzing the final step of bacterial fatty acid biosynthesis. A number of novel 2-pyridone derivatives were synthesized and shown to be potent inhibitors of
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