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Key Documents

565415

Sigma-Aldrich

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
MDL number:
UNSPSC Code:
12352108
PubChem Substance ID:
NACRES:
NA.22

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

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

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

Certificates of Analysis (COA)

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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

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