423971
Ethyl 4-pyridylacetate
97%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C9H11NO2
CAS Number:
Molecular Weight:
165.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
259-150-2
MDL number:
assay
97%
refractive index
n20/D 1.499 (lit.)
bp
127-128 °C/14 mmHg (lit.)
mp
18-19 °C (lit.)
density
1.079 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)Cc1ccncc1
InChI
1S/C9H11NO2/c1-2-12-9(11)7-8-3-5-10-6-4-8/h3-6H,2,7H2,1H3
InChI key
QVLJLWHOILVHJJ-UHFFFAOYSA-N
General description
Ethyl 4-pyridylacetate is an ethyl ester of 4-pyridyl acetic acid. Its hydrochloride salt was used to prepare the starting material required for the synthesis of 2,2-dideutero-1-azabicyclo(2,2,2)-octane. It participates as a reagent in the synthesis of triarylethane phosphodiesterase 4 inhibitors.
Application
Ethyl 4-pyridylacetate is a pyridine-based compound used for the grafting onto the self-adhesive gold substrates.
It may be used for the the following:
It may be used for the the following:
- As a starting material in the synthesis of 4-piperidylethanol.
- As a reactant in the synthesis of 4-(pyridyl) isosteres of meperidine.
- As a starting material in the synthesis of ethyl-4-piperidylacetate.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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.
CDP840. A prototype of a novel class of orally active anti-inflammatory phosphodiesterase 4 inhibitors.
Alexander RP, et al.
Bioorganic & Medicinal Chemistry Letters, 12(11), 1451-1456 (2002)
The Pyridylthioacetmorpholides and Pyridylacetic Acids.
Malan RL and Dean PM.
Journal of the American Chemical Society, 69(7), 1797-1798 (1947)
Synthesis and antinociceptive activity of 2-and 3-methyl derivatives of 4-(pyridyl) isosteres of meperidine.
Buolamwini JK and Knaus EE.
Drug Des. Discovery, 8(2), 145-156 (1991)