180696
Dimethyl 2-oxopropylphosphonate
95%
Synonym(s):
Dimethyl acetonylphosphonate
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CH3COCH2P(O)(OCH3)2
CAS Number:
Molecular Weight:
166.11
UNSPSC Code:
12352108
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-110-5
Beilstein/REAXYS Number:
1766218
MDL number:
Assay:
95%
Form:
liquid
InChI key
UOWIYNWMROWVDG-UHFFFAOYSA-N
InChI
1S/C5H11O4P/c1-5(6)4-10(7,8-2)9-3/h4H2,1-3H3
SMILES string
COP(=O)(CC(C)=O)OC
assay
95%
form
liquid
reaction suitability
reaction type: C-C Bond Formation
refractive index
n20/D 1.439 (lit.)
bp
76-79 °C/3 mmHg (lit.)
density
1.202 g/mL at 25 °C (lit.)
functional group
ketone, phosphonate
Quality Level
Related Categories
Application
Reagent used together with tosyl azide in a one-pot alkynylation of aldehydes.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
200.1 °F - closed cup
flash_point_c
93.4 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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.
Synthesis, 59-59 (2004)
Synthesis, 753-753 (2006)
B Resul et al.
Journal of medicinal chemistry, 36(2), 243-248 (1993-01-22)
A series of phenyl-substituted analogues of prostaglandin F2 alpha (PGF2 alpha) were prepared and evaluated for ocular hypotensive effect and side effects in different animal models. In addition, the activity of the analogues on FP receptors was studied in vitro.
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