物质信息
ID:357523
名称和标识
IUPAC标准名
methyl 2-(diethoxyphosphoryl)acetate
IUPAC传统名
methyl 2-(diethoxyphosphoryl)acetate
别名
(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
化合物性质
理化性质
闪点
110 °C
230 °F
折射率
n20/D 1.433(lit.)
n20/D 1.433
密度
1.145 g/mL at 25 °C(lit.)
沸点
127-131 °C/9 mmHg(lit.)
安全信息
欧盟危险性物质标志
刺激性 (Xi)GHS危险声明
H315-H319-H335
安全公开号
26-36
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
危险公开号
36/37/38
个人保护装置
Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
MSDS下载
GHS警示性声明
P261-P305+P351+P338
德国WGK号
3
GHS警示词
Warning
产品相关信息
纯度
≥95.0% (GC)
线性分子式
(C2H5O)2P(O)CH2CO2CH3
级别
purum
描述信息
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
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参考文献
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