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Methyl diethylphosphonoacetate, 97%, Thermo Scientific Chemicals
$111.40 - $1055.53
Chemical Identifiers
CAS | 1067-74-9 |
---|---|
Molecular Formula | C7H15O5P |
Molecular Weight (g/mol) | 210.166 |
MDL Number | MFCD00009081 |
InChI Key | CTSAXXHOGZNKJR-UHFFFAOYSA-N |
Synonym | methyl diethylphosphonoacetate, methyl 2-diethoxyphosphoryl acetate, acetic acid, diethoxyphosphinyl-, methyl ester, diethylmethylphosphonoacetate, methyl diethoxyphosphoryl acetate, diethyl carbomethoxymethylphosphonate, methyl 2-diethoxycarbonyl acetate, methyldiethylphosphonoacetate, diethyl methylphosphonoacetate, ksc489e0f |
PubChem CID | 66113 |
IUPAC Name | methyl 2-diethoxyphosphorylacetate |
SMILES | CCOP(=O)(CC(=O)OC)OCC |
Catalog Number | Mfr. No. | Quantity | Price | Quantity | ||||||
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Catalog Number | Mfr. No. | Quantity | Price | Quantity | ||||||
AAA1064414
|
Thermo Scientific Chemicals
A1064414 |
25 g |
Each for $111.40
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AAA1064422
|
Thermo Scientific Chemicals
A1064422 |
100 g |
Each for $315.93
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AAA1064436
|
Thermo Scientific Chemicals
A1064436 |
500 g |
Each for $1,055.53
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Description
Methyl diethylphosphonoacetate is used as a reagent in the preparation of allylic fluorides compounds and in regioselective Diels-Alder reactions. It also serves as a reactant in the preparation of substituted thiophenes and furans, which finds application in type 2 diabetes treatment. Further, it acts as a precursor in the synthesis of pyridone alkaloids and immunosuppressive cyclopentanediol derivatives. In addition to this, it is utilized in the modification of botulinum neurotoxin serotype A protease inhibitors.
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.
ApplicationsMethyl diethylphosphonoacetate is used as a reagent in the preparation of allylic fluorides compounds and in regioselective Diels-Alder reactions. It also serves as a reactant in the preparation of substituted thiophenes and furans, which finds application in type 2 diabetes treatment. Further, it acts as a precursor in the synthesis of pyridone alkaloids and immunosuppressive cyclopentanediol derivatives. In addition to this, it is utilized in the modification of botulinum neurotoxin serotype A protease inhibitors.
Solubility
Miscible with tetrahydrofuran.
Notes
Incompatible with strong oxidizing agents.
Chemical Identifiers
1067-74-9 | |
210.166 | |
CTSAXXHOGZNKJR-UHFFFAOYSA-N | |
66113 | |
CCOP(=O)(CC(=O)OC)OCC |
C7H15O5P | |
MFCD00009081 | |
methyl diethylphosphonoacetate, methyl 2-diethoxyphosphoryl acetate, acetic acid, diethoxyphosphinyl-, methyl ester, diethylmethylphosphonoacetate, methyl diethoxyphosphoryl acetate, diethyl carbomethoxymethylphosphonate, methyl 2-diethoxycarbonyl acetate, methyldiethylphosphonoacetate, diethyl methylphosphonoacetate, ksc489e0f | |
methyl 2-diethoxyphosphorylacetate |
Specifications
1067-74-9 | |
126°C to 128°C (8 mmHg) | |
C7H15O5P | |
MFCD00009081 | |
1782397 | |
Miscible with tetrahydrofuran. | |
CCOP(=O)(CC(=O)OC)OCC | |
210.166 | |
210.17 | |
Methyl diethylphosphonoacetate |
1.145 | |
>110°C (230°F) | |
1.432 | |
25 g | |
methyl diethylphosphonoacetate, methyl 2-diethoxyphosphoryl acetate, acetic acid, diethoxyphosphinyl-, methyl ester, diethylmethylphosphonoacetate, methyl diethoxyphosphoryl acetate, diethyl carbomethoxymethylphosphonate, methyl 2-diethoxycarbonyl acetate, methyldiethylphosphonoacetate, diethyl methylphosphonoacetate, ksc489e0f | |
CTSAXXHOGZNKJR-UHFFFAOYSA-N | |
methyl 2-diethoxyphosphorylacetate | |
66113 | |
97% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 213-938-2
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only