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Diethyl allylphosphonate_Molecular_structure_CAS_1067-87-4)
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Diethyl allylphosphonate

Catalog No. 565415 Name Sigma Aldrich
CAS Number 1067-87-4 Website http://www.sigmaaldrich.com
M. F. C7H15O3P Telephone 1-800-521-8956
M. W. 178.165961 Fax
Purity 98% Email
Storage Chembase ID: 74893

SYNONYMS

Title
烯丙基磷酸二乙酯
IUPAC name
diethyl (prop-2-en-1-yl)phosphonate
IUPAC Traditional name
diethyl prop-2-en-1-ylphosphonate
Synonyms
2-Propenyl-phosphonic acid diethyl ester

DATABASE IDS

PubChem SID 24880237
CAS Number 1067-87-4
MDL Number MFCD00015134

PROPERTIES

Bulk Density 1.022 g/mL
Linear Formula CH2=CHCH2P(O)(OC2H5)2
Purity 98%
Boiling Point 46 °C/0.35 mmHg(lit.)
Refractive Index n20/D 1.4340(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
5 g in glass bottle
Application
Reactant for:
• Copolymerization of phosphonated allyl monomers and maleic anhydride1
• Enantioselective synthesis of solamin type mono-THF acetogenins2
• RCM reaction yielding oxaphospholene and oxaphosphinene heterocycles3
• Synthesis of spongistatin 2 using Wittig coupling4
• Stereoselective synthesis of pentacyclic furanosteroids5
• Preparation of protected polyhydroxylated β -amino acid constitutents of microsclerodermins6
Description (简体中文)
包装
5 g in glass bottle
Application
Reactant for:
• Copolymerization of phosphonated allyl monomers and maleic anhydride1
• Enantioselective synthesis of solamin type mono-THF acetogenins2
• RCM reaction yielding oxaphospholene and oxaphosphinene heterocycles3
• Synthesis of spongistatin 2 using Wittig coupling4
• Stereoselective synthesis of pentacyclic furanosteroids5
• Preparation of protected polyhydroxylated β -amino acid constitutents of microsclerodermins6

REFERENCES