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Dimethyl 2-oxopropylphosphonate

Name: Dimethyl 2-oxopropylphosphonate
Brand: ALDRICH

95%

Synonym(s):

Dimethyl acetonylphosphonate

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About This Item

Linear Formula:

CH₃COCH₂P(O)(OCH₃)₂

CAS Number:

4202-14-6

Molecular Weight:

166.11

Beilstein:

1766218

EC Number:

224-110-5

MDL number:

MFCD00008769

UNSPSC Code:

12352108

PubChem Substance ID:

24850888

NACRES:

NA.22

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.)

SMILES string

COP(=O)(CC(C)=O)OC

InChI

1S/C5H11O4P/c1-5(6)4-10(7,8-2)9-3/h4H2,1-3H3

InChI key

UOWIYNWMROWVDG-UHFFFAOYSA-N

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Related Categories

C-C Bond Forming Reagents

Application

Reagent used together with tosyl azide in a one-pot alkynylation of aldehydes.

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis, 753-753 (2006)

Synthesis, 59-59 (2004)

Phenyl-substituted prostaglandins: potent and selective antiglaucoma agents.

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.

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