tert-Butyl diethylphosphonoacetate, 95%
tert-Butyl diethylphosphonoacetate, 95%
tert-Butyl diethylphosphonoacetate, 95%
Thermo Scientific Chemicals

tert-Butyl diethylphosphonoacetate, 95%

CAS: 27784-76-5 | C10H21O5P | 252.247 g/mol
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5 g
25 g
Catalog number L17651.06
also known as L17651-06
Price (USD)
90.65
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Ends: 30-Jun-2026
106.00
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Quantity:
5 g
Request bulk or custom format
Price (USD)
90.65
Special offer
Online exclusive
Ends: 30-Jun-2026
106.00
Save 15.35 (14%)
Each
Chemical Identifiers
CAS27784-76-5
IUPAC Nametert-butyl 2-(diethoxyphosphoryl)acetate
Molecular FormulaC10H21O5P
InChI KeyNFEGNISFSSLEGU-UHFFFAOYSA-N
SMILESCCOP(=O)(CC(=O)OC(C)(C)C)OCC
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless
Assay (GC)≥94.0%
FormLiquid
Refractive Index1.4285-1.4345 @ 20?C
tert-Butyl diethylphosphonoacetate is used as a reactant for preparation of hydroxymethylated dihydroxyvitamin D3 analogs via Wittig-Horner approach, as potential antitumor agents, synthesis of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat 3) and bicyclic triaminophosphine-promoted stereoselective synthesis of a,β-unsaturated esters, fluorides, and nitriles from aldehydes and ketones using Wadsworth-Emmons phosphonates

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
tert-Butyl diethylphosphonoacetate is used as a reactant for preparation of hydroxymethylated dihydroxyvitamin D3 analogs via Wittig-Horner approach, as potential antitumor agents, synthesis of phosphopeptide mimetic prodrugs targeted to Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 (Stat 3) and bicyclic triaminophosphine-promoted stereoselective synthesis of a,ß-unsaturated esters, fluorides, and nitriles from aldehydes and ketones using Wadsworth-Emmons phosphonates

Solubility
Not miscible or difficult to mix in water.

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Pijus K Mandal.; Fengqin Gao.; Zhen Lu.; Zhiyong Ren.; Rajagopal Ramesh.; J Sanderson Birtwistle.; Kumaralal K Kaluarachchi.; Xiaomin Chen.; Robert C Bast.; Warren S Liao.; John S McMurray. Potent and selective phosphopeptide mimetic prodrugs targeted to the Src homology 2 (SH2) domain of signal transducer and activator of transcription 3 . Journal of medicinal and pharmaceutical chemistry. 2011, 54 (10), 3549-3563.
  2. Maria A Regueira.; Shaonly Samanta.; Peter J Malloy.; Paloma Ordonez-Moran.; Diana Resende.; Fredy Sussman.; Alberto Munoz.; Antonio Mourino.; David Feldman.; Mercedes Torneiro. Synthesis and biological evaluation of 1α,25-dihydroxyvitamin D(3) analogues hydroxymethylated at C-26. Langmuir. 2011, 54 (11), 3950-3962.