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Triethyl 4-phosphonocrotonate, cis + trans, 94%, Thermo Scientific Chemicals
$199.05 - $372.53
Chemical Identifiers
| CAS | 10236-14-3 |
|---|---|
| Molecular Formula | C10H19O5P |
| Molecular Weight (g/mol) | 250.23 |
| MDL Number | MFCD00009192 |
| InChI Key | LXLODBXSCRTXFG-BQYQJAHWSA-N |
| Synonym | triethyl 4-phosphonocrotonate, e-ethyl 4-diethoxyphosphoryl but-2-enoate, ethyl 4-diethoxyphosphoryl but-2-enoate, triethyl .gamma.-phosphonocrotonate, ethyl 4-diethylphosphono crotonate, ethyl 2e-4-diethoxyphosphoryl but-2-enoate, ethyl e-4-diethoxyphosphorylbut-2-enoate, ethyl 4-diethylphosphonocrotonate, ethyl trans-4-diethylphosphono crotonate, 4-diethoxyphosphinyl crotonic acid ethyl ester |
| PubChem CID | 5365783 |
| IUPAC Name | ethyl (E)-4-diethoxyphosphorylbut-2-enoate |
| SMILES | CCOC(=O)\C=C\CP(=O)(OCC)OCC |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1099509
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Thermo Scientific Chemicals
A1099509 |
10 g |
Each for $199.05
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AAA1099514
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Thermo Scientific Chemicals
A1099514 |
25 g |
Each for $372.53
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Description
Triethyl 4-phosphonocrotonate is used as a reactant for iminodipropionic acid as a leaving group for DNA polymerization by HIV-1 reverse transcriptase, orally bioavailable GPR40 agonist synthesis, preparation of mGlu4R agonists and synthesis of fluoroketone inhibitors of group VIA calcium-independent phospholipase A2.
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.
ApplicationsTriethyl 4-phosphonocrotonate is used as a reactant for iminodipropionic acid as a leaving group for DNA polymerization by HIV-1 reverse transcriptase, orally bioavailable GPR40 agonist synthesis, preparation of mGlu4R agonists and synthesis of fluoroketone inhibitors of group VIA calcium-independent phospholipase A2.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Chemical Identifiers
| 10236-14-3 | |
| 250.23 | |
| LXLODBXSCRTXFG-BQYQJAHWSA-N | |
| 5365783 | |
| CCOC(=O)\C=C\CP(=O)(OCC)OCC |
| C10H19O5P | |
| MFCD00009192 | |
| triethyl 4-phosphonocrotonate, e-ethyl 4-diethoxyphosphoryl but-2-enoate, ethyl 4-diethoxyphosphoryl but-2-enoate, triethyl .gamma.-phosphonocrotonate, ethyl 4-diethylphosphono crotonate, ethyl 2e-4-diethoxyphosphoryl but-2-enoate, ethyl e-4-diethoxyphosphorylbut-2-enoate, ethyl 4-diethylphosphonocrotonate, ethyl trans-4-diethylphosphono crotonate, 4-diethoxyphosphinyl crotonic acid ethyl ester | |
| ethyl (E)-4-diethoxyphosphorylbut-2-enoate |
Specifications
| 10236-14-3 | |
| 133°C to 135°C (0.4 mmHg) | |
| C10H19O5P | |
| MFCD00009192 | |
| triethyl 4-phosphonocrotonate, e-ethyl 4-diethoxyphosphoryl but-2-enoate, ethyl 4-diethoxyphosphoryl but-2-enoate, triethyl .gamma.-phosphonocrotonate, ethyl 4-diethylphosphono crotonate, ethyl 2e-4-diethoxyphosphoryl but-2-enoate, ethyl e-4-diethoxyphosphorylbut-2-enoate, ethyl 4-diethylphosphonocrotonate, ethyl trans-4-diethylphosphono crotonate, 4-diethoxyphosphinyl crotonic acid ethyl ester | |
| CCOC(=O)\C=C\CP(=O)(OCC)OCC | |
| 250.23 | |
| 250.23 | |
| Triethyl 4-phosphonocrotonate, cis + trans |
| 1.13 | |
| >110°C (230°F) | |
| 1.455 | |
| 10 g | |
| LXLODBXSCRTXFG-BQYQJAHWSA-N | |
| ethyl (E)-4-diethoxyphosphorylbut-2-enoate | |
| 5365783 | |
| 94% |
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
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only