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565415

Diethyl allylphosphonate

98%

Synonym(s):

2-Propenyl-phosphonic acid diethyl ester

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About This Item

Linear Formula:
CH2=CHCH2P(O)(OC2H5)2
CAS Number:
Molecular Weight:
178.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352108
MDL number:
Assay:
98%
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Quality Level

assay

98%

reaction suitability

reaction type: C-C Bond Formation

refractive index

n20/D 1.4340 (lit.)

bp

46 °C/0.35 mmHg (lit.)

bulk density

1.022 g/mL

functional group

phosphonate

SMILES string

CCOP(=O)(CC=C)OCC

InChI

1S/C7H15O3P/c1-4-7-11(8,9-5-2)10-6-3/h4H,1,5-7H2,2-3H3

InChI key

YPJHXRAHMUKXAE-UHFFFAOYSA-N

Application

Reactant for:
  • Copolymerization of phosphonated allyl monomers and maleic anhydride
  • Enantioselective synthesis of solamin type mono-THF acetogenins
  • RCM reaction yielding oxaphospholene and oxaphosphinene heterocycles
  • Synthesis of spongistatin 2 using Wittig coupling
  • Stereoselective synthesis of pentacyclic furanosteroids
  • Preparation of protected polyhydroxylated β -amino acid constitutents of microsclerodermins

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This Item
D91705411361392626
assay

98%

assay

98%

assay

96%

assay

-

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

reaction suitability

reaction type: C-C Bond Formation

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

refractive index

n20/D 1.4340 (lit.)

refractive index

n20/D 1.434 (lit.)

refractive index

n20/D 1.417 (lit.)

refractive index

n20/D 1.444 (lit.)

bp

46 °C/0.35 mmHg (lit.)

bp

101-102 °C/0.4 mmHg (lit.)

bp

40-41 °C/0.05 mmHg (lit.)

bp

124-126 °C/3 mmHg (lit.)

bulk density

1.022 g/mL

bulk density

-

bulk density

-

bulk density

-


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



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Elizabeth I Parkinson et al.
Nature chemical biology, 15(11), 1049-1056 (2019-08-28)
Fosmidomycin and related molecules comprise a family of phosphonate natural products with potent antibacterial, antimalarial and herbicidal activities. To understand the biosynthesis of these compounds, we characterized the fosmidomycin producer, Streptomyces lavendulae, using biochemical and genetic approaches. We were unable



Global Trade Item Number

SKUGTIN
565415-5G04061833356135

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