2526-67-2

Basic information

• Product Name: diethyl 3-aMino-3-oxopropylphosphonate
• Synonyms: diethyl 3-aMino-3-oxopropylphosphonate
• CAS NO: 2526-67-2
• Molecular Formula: C₇H₁₆NO₄P
• Molecular Weight: 209.180001
• Mol File: 2526-67-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: diethyl 3-aMino-3-oxopropylphosphonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 3-aMino-3-oxopropylphosphonate(2526-67-2)
• EPA Substance Registry System: diethyl 3-aMino-3-oxopropylphosphonate(2526-67-2)

Safety Data

• Hazardous Substances Data: 2526-67-2(Hazardous Substances Data)

Upstream product

• 3699-67-0 ethyl 3-(diethoxyphosphoryl)propanoate 
• 1112-94-3 methyl 3-(diethoxyphosphinyl)-propanoate 
• 79-06-1 2-propenamide 
• 122-52-1 triethyl phosphite 
• 762-04-9 phosphonic acid diethyl ester 

Downstream Products

• 41468-36-4 diethyl (2-aminoethyl)phosphonate 
• 4402-24-8 diethyl 3-aminopropan-1-ylphosphonate 

Relevant articles and documents

Comparison of catalytic activity of hexamethyltriamino- and tri-n-butylphosphines in the Pudovik reaction

The catalytic activity of hexamethyltriaminophosphine in the P(O)–H bond addition to electron-deficient alkenes was studied. Depending on the nature of the alkene, hexamethyltriaminophosphine produces better or lower yields of the reaction products compared to tri-n-butylphosphine.

One-pot synthesis of γ-hydroxy-γ-oxaphosphonates using pentacovalent oxaphosphorane chemistry

P(V)-2,2,2-triethoxy-2,2-dihydro-5-methoxy-1,2λ5-oxaphospholene was synthesized as a new type of enolate which was hydrolyzed to give a series of phosphonates. In addition, aldol reaction of the oxaphospholene intermediate with several aldehyde

Application of Hypervalent Iodine Reagents to the Synthesis of Aminophosphonic Acids

-