36871-68-8 Usage
Uses
Used in Organic Synthesis:
(Benzylphosphoryl)bis(phenylmethanol) is used as a reagent in organic synthesis for its ability to facilitate the formation of phosphoester bonds. These bonds are crucial in the synthesis of nucleic acids and other biologically relevant molecules, making (benzylphosphoryl)bis(phenylmethanol) an essential tool in the creation of various pharmaceuticals and fine chemicals.
Used in Pharmaceutical Production:
As a chemical intermediate, (benzylphosphoryl)bis(phenylmethanol) plays a significant role in the production of a wide range of pharmaceuticals. Its involvement in the synthesis of nucleic acids and other biological molecules contributes to the development of new drugs and therapeutic agents.
Used in Material Science:
Due to its unique structural and chemical properties, (benzylphosphoryl)bis(phenylmethanol) has been studied for potential applications in material science. Its use in this field could lead to the development of novel materials with specific properties tailored for various applications.
Used in Catalysis:
(benzylphosphoryl)bis(phenylmethanol) has also been investigated for its potential use in catalysis, where it could be employed to enhance the efficiency of chemical reactions. This application could further expand the utility of (benzylphosphoryl)bis(phenylmethanol) in the chemical industry and beyond.
Check Digit Verification of cas no
The CAS Registry Mumber 36871-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,7 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 36871-68:
(7*3)+(6*6)+(5*8)+(4*7)+(3*1)+(2*6)+(1*8)=148
148 % 10 = 8
So 36871-68-8 is a valid CAS Registry Number.
36871-68-8Relevant academic research and scientific papers
Phosphorylating power of red phosphorus towards aldehydes in basic and in acidic media
Albouy, Dominique,Etemad-Moghadam, Guita,Koenig, Max
, p. 861 - 868 (2007/10/03)
The reactivity of red phosphorus towards aldehydes was investigated under basic and acidic media. It was demonstrated that the real phosphorylating agent involved in the reaction was phosphane (PH3) in basic media, and hypophosphorous acid (H3PO2) in acidic media. A convenient one- pot synthesis of (α-hydroxyalkyl)phosphinic acids from red phosphorus and aldehydes in basic media was realized under sonication. The same reaction under acidic media in the presence of hydriodic acid led to the corresponding phosphonic acids. The (α-hydroxyalkyl) phosphinic acids were readily prepared under sonication from hypophosphorous acid and aldehydes in the presence of catalytic amounts of hydrochloric acid. The mechanism of the addition reaction of PH3 to benzaldehyde was elucidated and shows the complexity of the reaction as a function of the experimental conditions.
