101040-15-7 Usage
Uses
Used in Organic Synthesis:
(+)-(S)-diethyl 2-benzyloxy-1-(hydroxyamino)ethylphosphonate is used as a reagent in organic synthesis for the preparation of peptide and protein derivatives. Its unique structure allows for the creation of complex organic molecules that are essential in various chemical and pharmaceutical processes.
Used in Pharmaceutical Compounds:
As a building block, (+)-(S)-diethyl 2-benzyloxy-1-(hydroxyamino)ethylphosphonate is utilized in the synthesis of a variety of pharmaceutical compounds. Its versatility in forming stable bonds with other molecules makes it a valuable component in the development of new drugs.
Used in Antimicrobial Applications:
(+)-(S)-diethyl 2-benzyloxy-1-(hydroxyamino)ethylphosphonate has been investigated for its antimicrobial properties, making it a potential candidate for use in the development of new antimicrobial agents to combat resistant strains of bacteria.
Used in Antiproliferative Applications:
(+)-(S)-diethyl 2-benzyloxy-1-(hydroxyamino)ethylphosphonate has also shown antiproliferative properties, indicating its potential use in the development of treatments for conditions characterized by uncontrolled cell growth, such as cancer. Further research is needed to fully understand its mechanism of action and therapeutic potential in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 101040-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,4 and 0 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101040-15:
(8*1)+(7*0)+(6*1)+(5*0)+(4*4)+(3*0)+(2*1)+(1*5)=37
37 % 10 = 7
So 101040-15-7 is a valid CAS Registry Number.
101040-15-7Relevant academic research and scientific papers
181. Nuchleophilic Additions to N-Glycosylnitrones Asymmetric Synthesis of α-Aminophosphonic Acids
Huber, Rolf,Knierzinger, Andreas,Obrecht, Jean-Pierre,Vasella, Andrea
, p. 1730 - 1747 (2007/10/02)
The hypothesis which explains the diastereoselectivity of the 1,3-dipolar cycloaddition of the N-glycosylnitrones 1-3 leading to the 5,5-disubstituted isoxazolidines 4-6 on the basis of a kinetic anomeric effect predicts that nucleophiles should add to N-
