410616
4-Benzyloxy-2(1H)-pyridone
99%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C12H11NO2
CAS Number:
Molecular Weight:
201.22
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
assay
99%
form
solid
mp
201-203 °C (lit.)
SMILES string
O=C1NC=CC(OCc2ccccc2)=C1
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)
InChI key
DOVNUEPFPBWTSV-UHFFFAOYSA-N
General description
N-alkylation of 4-benzyloxy-2(1H)-pyridone with the corresponding benzyl halides has been reported.
Application
4-Benzyloxy-2(1H)-pyridone may be used for the synthesis of novel 2-pyridone derivatives. It may be used for the alkylation of the pyridine nitrogen under mild and anhydrous conditions, via reaction with n-Bu4I and KOBu-t.†
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 410616-1G | 04061832019581 |
| 410616-5G | 04061832545011 |