89429-98-1 Usage
Uses
Used in Organic Synthesis:
Phosphonic acid, [hydroxy(2-nitrophenyl)methyl]-, dimethyl ester, (S)is utilized as a starting material in the synthesis of a range of organic compounds. Its unique structure allows for the creation of diverse chemical entities, making it a valuable component in organic chemistry.
Used as a Chelating Agent in Chemical Processes:
In various chemical processes, Phosphonic acid, [hydroxy(2-nitrophenyl)methyl]-, dimethyl ester, (S)serves as an effective chelating agent for metal ions. Its ability to form stable complexes with metals is crucial for applications where metal ion management is necessary, such as in catalysis or the stabilization of reactive intermediates.
Used in Pharmaceutical Industry:
Phosphonic acid, [hydroxy(2-nitrophenyl)methyl]-, dimethyl ester, (S)may be employed in the pharmaceutical industry as a building block for the development of new drugs. Its versatile chemical structure can be modified to target specific biological pathways or to improve the pharmacokinetic properties of drug candidates.
Used in Material Science:
In the field of material science, Phosphonic acid, [hydroxy(2-nitrophenyl)methyl]-, dimethyl ester, (S)can be incorporated into the design of new materials with tailored properties. Its ability to interact with metal ions and form stable structures makes it a candidate for use in the development of advanced materials with applications in areas such as sensors, catalysts, or coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 89429-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,2 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89429-98:
(7*8)+(6*9)+(5*4)+(4*2)+(3*9)+(2*9)+(1*8)=191
191 % 10 = 1
So 89429-98-1 is a valid CAS Registry Number.
89429-98-1Relevant academic research and scientific papers
Organic catalysis of phospha-aldol condensation
Kolodyazhnaya,Kukhar,Kolodyazhnyi
experimental part, p. 2043 - 2051 (2009/04/13)
Phospha-aldol reaction of dialkylphosphites with carbonyl compounds is catalyzed by cinchonine alkaloids and thier modified derivatives to give optically active hydroxyphosphonates. The use of diastereomeric pairs of alkaloids allowed obtaining both optic
THE ABSOLUTE CONFIGURATION OF α-HYDROXYPHOSPHONATES
Smaardijk, Ab. A.,Noorda, Simon,Bolhuis, Fre van,Wynberg, Hans
, p. 493 - 496 (2007/10/02)
The absolute configuration and CD spectra of a series of chiral α-hydroxyphosphonates and phosphoric acids have been determinated.The hydroxyphosphonates were prepared via a quinine catalyzed 1,2-addition reaction of phosphite to aldehyde.
ASYMMERIC CATALYSIS IN CARBON-PHOSPHORUS BOND FORMATION
Wynberg, Hans,Smaardijk, Ab A.
, p. 5899 - 5900 (2007/10/02)
o-Nitrobenzaldehyde reacts smoothly with dialkylphosphonates in the presence of catalytic quantities of cinchona alkaloids (e.g.quinine) to produce the α-hydroxy phosphonate esters in excellent chemical yields, with excellent enantiomeric enrichment.
