Diethyl 2-bromoethylphosphonate

• Catalog No.: 16148
• CAS Number: 5324-30-1
• M. F.: C6H14BrO3P
• M. W.: 245.051321
• Purity: ≥97.0% (GC)

SYNONYMS

• Title: 2-溴乙基膦酸二乙酯
• IUPAC name: diethyl (2-bromoethyl)phosphonate
• IUPAC Traditional name: diethyl 2-bromoethylphosphonate
• Synonyms: NSC 119421; NSC 2672; (2-Bromoethyl)phosphonic acid diethyl ester

DATABASE IDS

• PubChem SID: 24849931
• CAS Number: 5324-30-1
• EC Number: 226-193-3
• Beilstein Number: 1766077
• MDL Number: MFCD00000239

PROPERTIES

• Grade: purum
• Linear Formula: BrCH2CH2P(O)(OCH2CH3)2
• Purity: ≥97.0% (GC)
• Boiling Point: 75 °C/1 mmHg(lit.)
• Density: 1.348 g/mL at 25 °C(lit.)
• Flash Point: 110 °C
• Flash Point: 230 °F
• Refractive Index: n20/D 1.461(lit.)
• Refractive Index: n20/D 1.461
• Personal Protective Equipment: Eyeshields, Gloves
• German water hazard class: 3

DETAILS

Description (English)

Other Notes
Synthesis of N-substit. 2-aminoethylphosphonic acids7,8,9; Prep. of zinc-copper reagent and reaction with electrophiles10
Application
Reactant involved in:
• Radical coupling1
• Synthesis of organosoluble zirconium phosphonate nanocomposites2
• Click-chemistry3
• Asymmetric epoxidation of unfunctionalized olefins4
• Negishi alkyl-aryl cross-coupling5
• Synthesis of hydrolytically stable phosphonic acids for use as dental adhesives6

Description (简体中文)

Other Notes
合成 N-取代 2-氨基乙基膦酸7,8,9；锌-铜试剂的制备以及与亲电试剂的反应10
Application
Reactant involved in:
• Radical coupling1
• Synthesis of organosoluble zirconium phosphonate nanocomposites2
• Click-chemistry3
• Asymmetric epoxidation of unfunctionalized olefins4
• Negishi alkyl-aryl cross-coupling5
• Synthesis of hydrolytically stable phosphonic acids for use as dental adhesives6