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180696

Sigma-Aldrich

Dimethyl 2-oxopropylphosphonate

95%

Synonym(s):

Dimethyl acetonylphosphonate

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5 G
¥5,530
25 G
¥32,100

¥5,530

Estimated to ship onMarch 22, 2025

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5 G
¥5,530
25 G
¥32,100

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

¥5,530

Estimated to ship onMarch 22, 2025

Request a Bulk Order

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

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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Application

Reagent used together with tosyl azide in a one-pot alkynylation of aldehydes.[1][2]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

200.1 °F - closed cup

Flash Point(C)

93.4 °C - closed cup

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.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

180696-1G:
180696-BULK:
180696-VAR:
180696-25G:
180696-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
0000368221
0000313320
0000311465
0000313320
0000311465

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Sigma-Aldrich

158755

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Synthesis, 753-753 (2006)
Synthesis, 59-59 (2004)
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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