All Photos(1)
About This Item
Linear Formula:
C6H5COP(O)(OC2H5)2
CAS Number:
Molecular Weight:
242.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
97%
refractive index
n20/D 1.508 (lit.)
bp
186 °C (lit.)
density
1.156 g/mL at 25 °C (lit.)
functional group
phenyl
phosphonate
SMILES string
CCOP(=O)(OCC)C(=O)c1ccccc1
InChI
1S/C11H15O4P/c1-3-14-16(13,15-4-2)11(12)10-8-6-5-7-9-10/h5-9H,3-4H2,1-2H3
InChI key
TZAMQIAPGYOUKF-UHFFFAOYSA-N
Related Categories
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
Choose from one of the most recent versions:
Certificates of Analysis (COA)
Lot/Batch Number
Don't see the Right Version?
If you require a particular version, you can look up a specific certificate by the Lot or Batch number.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Studies on pyrimidine derivatives and related compounds. XLI. Reaction of diethyl benzoylphosphonate with thiamine (Takamizawa reaction 3).
A Takamizawa et al.
The Journal of organic chemistry, 31(9), 2951-2956 (1966-09-01)
Diethyl benzoylphosphonate as a ligand.
Mikulski CM, et al.
Transition Met. Chem. (London), 2(1), 135-140 (1977)
Asymmetric Hydrogenation of a, ?-Unsaturated Ester-Phosphonates.
Huang Y, et al.
Advanced Synthesis & Catalysis, 351(9), 1423-1430 (2009)
Characterization of polymeric metal complexes formed by reaction of excess diethyl acetyl-or diethyl benzoyl-phosphonate with metal chlorides at elevated temperatures.
Mikulski CM, et al.
J. Inorg. Nucl. Chem., 43(11), 2753-2757 (1981)
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