Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3CH2COCH2COOC2H5
CAS Number:
Molecular Weight:
144.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
225-593-5
Beilstein/REAXYS Number:
970270
MDL number:
Assay:
97%
Form:
liquid
InChI key
UDRCONFHWYGWFI-UHFFFAOYSA-N
InChI
1S/C7H12O3/c1-3-6(8)5-7(9)10-4-2/h3-5H2,1-2H3
SMILES string
CCOC(=O)CC(=O)CC
assay
97%
form
liquid
refractive index
n20/D 1.422 (lit.)
bp
83-84 °C/12 mmHg (lit.)
density
1.012 g/mL at 25 °C (lit.)
functional group
ester, ketone
Quality Level
Related Categories
General description
Ethyl propionylacetate reacts with tropolone p-toluenesulfonate in the presence of sodium ethoxide to give 3-propionyl-2H-cyclohepta[b]furan-2-one.
Application
Ethyl propionylacetate has been used in the synthesis of 1-ethyl- and 1-n-propyl-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid bearing one or two substituents on the benzene ring.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
172.4 °F - closed cup
flash_point_c
78 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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.
A simple and efficient synthesis of 2-alkylazulenes.
Iwama N, et al.
Tetrahedron Letters, 45(50), 9211-9213 (2004)
R R Martel et al.
Journal of medicinal chemistry, 19(3), 391-395 (1976-03-01)
A series of 37 1-ethyl- and 1-n-propyl-1, 3, 4, 9-tetrahydropyrano[3, 4-b]indole-1-acetic acids bearing one, or two, substituents on the benzene ring has been synthesized via the acid-catalyzed condensation of a substituted tryptophol with ethyl propionylacetate or ethyl butyrylacetate. Antiinflammatory and
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service