Methyl P,P-diethylphosphonoacetate

• Catalog No.: 79517
• CAS Number: 1067-74-9
• M. F.: C7H15O5P
• M. W.: 210.164761
• Purity: ≥95.0% (GC)

SYNONYMS

• Title: P,P-膦酰基乙酸甲酯二乙酯
• IUPAC name: methyl 2-(diethoxyphosphoryl)acetate
• IUPAC Traditional name: methyl 2-(diethoxyphosphoryl)acetate
• Synonyms: (Methoxycarbonylmethyl) diethoxyphosphine oxide; NSC 147757; [(Methoxycarbonyl)methyl]phosphonic acid diethyl ester

DATABASE IDS

• Beilstein Number: 1782397
• CAS Number: 1067-74-9
• MDL Number: MFCD00009081
• EC Number: 213-938-2

PROPERTIES

• Grade: purum
• Linear Formula: (C2H5O)2P(O)CH2CO2CH3
• Purity: ≥95.0% (GC)
• Boiling Point: 127-131 °C/9 mmHg(lit.)
• Density: 1.145 g/mL at 25 °C(lit.)
• Flash Point: 110 °C
• Flash Point: 230 °F
• Refractive Index: n20/D 1.433(lit.)
• Refractive Index: n20/D 1.433
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• 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
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

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

Description (简体中文)

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