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448796

Sigma-Aldrich

Diethyl benzoylphosphonate

97%

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1 G
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1 G
¥7,580

About This Item

Linear Formula:
C6H5COP(O)(OC2H5)2
CAS Number:
3277-27-8
Molecular Weight:
242.21
MDL number:
MFCD00015137
UNSPSC Code:
12352100
PubChem Substance ID:
24868432
NACRES:
NA.22

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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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

448796-VAR:
448796-10G:
448796-BULK:
448796-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
06025DQ

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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)
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)

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