Substance
ID:357523
Names and Identifiers
IUPAC name
methyl 2-(diethoxyphosphoryl)acetate
IUPAC Traditional name
methyl 2-(diethoxyphosphoryl)acetate
Synonyms
(Methoxycarbonylmethyl) diethoxyphosphine oxideNSC 147757[(Methoxycarbonyl)methyl]phosphonic acid diethyl esterP,P-膦酰基乙酸甲酯二乙酯Methyl P,P-diethylphosphonoacetate
Registration numbers
CAS Number
MDL Number
Beilstein Number
EC Number
Properties
Safety Information
GHS Signal Word
Warning
European Hazard Symbols
Irritant (Xi)GHS Hazard statements
H315-H319-H335
MSDS Link
German water hazard class
3
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
Safety Statements
26-36
Risk Statements
36/37/38
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
Product Information
Grade
purum
Linear Formula
(C2H5O)2P(O)CH2CO2CH3
Purity
≥95.0% (GC)
Physical Property
Refractive Index
n20/D 1.433(lit.)
n20/D 1.433
Flash Point
110 °C
230 °F
Density
1.145 g/mL at 25 °C(lit.)
Boiling Point
127-131 °C/9 mmHg(lit.)
Molecule Details
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
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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