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Diethyl (hydroxymethyl)phosphonate

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Products Intro: Product Name:Diethyl (hydroxymethyl)phosphonate
CAS:3084-40-0
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CAS:3084-40-0
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CAS:3084-40-0
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Products Intro: Product Name:Diethyl (Hydroxymethyl)Phosphonate
CAS:3084-40-0

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Diethyl (hydroxymethyl)phosphonate Basic information
Product Name:Diethyl (hydroxymethyl)phosphonate
Synonyms:AURORA KA-1421;DIETHYL HYDROXYMETHYLPHOSPHONATE;(Hydroxymethyl)phosphonic acid, diethyl ester;(hydroxymethyl)-phosphonicacidiethylester;Phosphonic acid, (hydroxymethyl)-, diethyl ester;4-Hydroxymethyldiethylphosphonate;DIETHYL (HYDROXYMETHYL)PHOSPHONATE, TECH .;Diethyl Phosphonometanol
CAS:3084-40-0
MF:C5H13O4P
MW:168.13
EINECS:221-391-6
Product Categories:C-C Bond Formation;Horner-Wadsworth-Emmons Reagents;Olefination
Mol File:3084-40-0.mol
Diethyl (hydroxymethyl)phosphonate Structure
Diethyl (hydroxymethyl)phosphonate Chemical Properties
Boiling point 124-126 °C/3 mmHg (lit.)
density 1.14 g/mL at 25 °C (lit.)
refractive index n20/D 1.444(lit.)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Viscous Liquid
pka13.00±0.10(Predicted)
color Clear colorless to yellow
Water Solubility 500g/L at 20℃
InChIKeyRWIGWWBLTJLKMK-UHFFFAOYSA-N
CAS DataBase Reference3084-40-0(CAS DataBase Reference)
NIST Chemistry ReferenceDiethyl hydroxymethylphosphonate(3084-40-0)
EPA Substance Registry SystemPhosphonic acid, (hydroxymethyl)-, diethyl ester (3084-40-0)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 37/39-26-36-37
WGK Germany 3
TSCA Yes
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
Diethyl (hydroxymethyl)phosphonate Usage And Synthesis
Chemical PropertiesClear colorless to yellow viscous liquid
UsesDiethyl hydroxymethylphosphonate acts as a reactant for synthesis of α And β-dialkoxyphosphoryl isothiocyanate used in antiproliferative studies, dendritic polyglycerol anions for L-selectin inhibition, phosphonates for anti-HIV-1 activity, homo and copolymers of phosphonated norbornenes, Mitsunobu reactions. It is involved in studies of FBPase inhibition by phosphonic acid-containing thaizoles.
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