2526-69-4 Usage
Description
Dimethyl (3-amino-3-oxopropyl)phosphonate is a phosphonate compound with the molecular formula C5H12NO4P. It contains both a phosphorus and an amine functional group, making it a versatile molecule with potential applications in various fields.
Uses
Used in Chelating Agents:
Dimethyl (3-amino-3-oxopropyl)phosphonate is used as a chelating agent for its ability to bind metal ions. This property makes it useful in various applications, such as water treatment, where it can help remove heavy metals from contaminated water sources.
Used in Medicinal Chemistry:
Dimethyl (3-amino-3-oxopropyl)phosphonate is used as a ligand for metal ions in medicinal chemistry. Its ability to bind metal ions can be utilized in the development of metal-based drugs, which have potential applications in the treatment of various diseases.
Used in Organic Synthesis:
Dimethyl (3-amino-3-oxopropyl)phosphonate is used as a precursor in the synthesis of other phosphonate compounds. Its unique structure and functional groups make it a valuable building block for the development of new organic compounds with potential applications in various industries.
Used in Research:
Dimethyl (3-amino-3-oxopropyl)phosphonate is used as a subject of interest for further research in various fields, including chemistry, biology, and materials science. Its unique properties and potential applications make it a promising candidate for the development of new technologies and products.
Check Digit Verification of cas no
The CAS Registry Mumber 2526-69-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2526-69:
(6*2)+(5*5)+(4*2)+(3*6)+(2*6)+(1*9)=84
84 % 10 = 4
So 2526-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H12NO4P/c1-9-11(8,10-2)4-3-5(6)7/h3-4H2,1-2H3,(H2,6,7)
2526-69-4Relevant articles and documents
The synthesis of dialkoxyphosphorylcarboxamides
Ye, Yong,Li, Ping,Hu, Xiao-Lian,Ju, Zhi-Yu,Zhao, Yu-Fen
, p. 701 - 705 (2008)
The synthesis of dialkoxyphosphorylcarboxamides, which is difficult to monitor by TLC, was investigated by ESI-MS and ESI-MSn. Their fragmentation pathways were rationalized and supported by tandem mass spectrometry. The characteristic ions in ESI-MS are