Substance
ID:337074
Names and Identifiers
IUPAC name
methyl 2-(diethoxyphosphoryl)acetate
IUPAC Traditional name
methyl 2-(diethoxyphosphoryl)acetate
Synonyms
Methyl diethylphosphonoacetate(Methoxycarbonylmethyl) diethoxyphosphine oxideNSC 147757[(Methoxycarbonyl)methyl]phosphonic acid diethyl esterMethyl P,P-diethylphosphonoacetateP,P-膦酰基乙酸甲酯二乙酯膦酰基乙酸甲酯二乙酯
Registration numbers
CAS Number
PubChem SID
MDL Number
Beilstein Number
EC Number
Properties
Product Information
Purity
97%
Linear Formula
(C2H5O)2P(O)CH2CO2CH3
Physical Property
Density
1.145 g/mL at 25 °C(lit.)
Flash Point
230 °F
110 °C
Boiling Point
127-131 °C/9 mmHg(lit.)
Refractive Index
n20/D 1.433(lit.)
Safety Information
GHS Signal Word
Warning
Safety Statements
26-36
European Hazard Symbols
Irritant (Xi)German water hazard class
3
GHS Hazard statements
H315-H319-H335
Risk Statements
36/37/38
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
MSDS Link
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
Molecule Details
Packaging
10, 50 g in glass bottle
Application
Reactant or reagent for:
• Synthesis of branches allylic fluorides1
• Regioselective Diels-Alder reactions to yield antibiotic building blocks2
• Substituted thiophenes and furans synthesis for treatment of type 2 diabetes3
• Stereoselective Diels-Alder cycloaddition reactions4
• Synthesis of pyridone alkaloids with neuritogenic activity5
• Modification of botulinum neurotoxin serotype A protease inhibitors6
• Synthesis of immunosuppressive cyclopentanediol derivatives7
10, 50 g in glass bottle
Application
Reactant or reagent for:
• Synthesis of branches allylic fluorides1
• Regioselective Diels-Alder reactions to yield antibiotic building blocks2
• Substituted thiophenes and furans synthesis for treatment of type 2 diabetes3
• Stereoselective Diels-Alder cycloaddition reactions4
• Synthesis of pyridone alkaloids with neuritogenic activity5
• Modification of botulinum neurotoxin serotype A protease inhibitors6
• Synthesis of immunosuppressive cyclopentanediol derivatives7
Molecular Spectra
No Data Available
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References
No Data Available
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