73451-43-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
DEPSS is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its unique chemical structure allows for the development of new drugs and pesticides with improved efficacy and reduced side effects.
Used as an Antimicrobial and Antifungul Agent:
DEPSS is used as an antimicrobial and antifungal agent due to its ability to inhibit the growth of harmful microorganisms. This makes it a valuable component in the development of new treatments for bacterial and fungal infections.
Used in Enzyme Inhibition:
DEPSS has been studied for its potential as an enzyme inhibitor, which can be useful in the development of drugs targeting specific enzymes involved in various diseases. By inhibiting these enzymes, DEPSS may contribute to the development of novel therapeutic strategies.
Used as a Precursor in the Synthesis of Novel Organic Compounds:
DEPSS serves as a valuable precursor in the synthesis of new organic compounds, expanding the range of chemical structures and functionalities that can be achieved. This can lead to the discovery of new materials with unique properties and applications.
Used in the Development of New Materials and Polymers:
DEPSS has been explored for its potential use in the development of new materials and polymers, which can be applied in various industries, such as electronics, automotive, and aerospace. The unique properties of DEPSS can contribute to the creation of advanced materials with improved performance and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 73451-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73451-43:
(7*7)+(6*3)+(5*4)+(4*5)+(3*1)+(2*4)+(1*3)=121
121 % 10 = 1
So 73451-43-1 is a valid CAS Registry Number.
73451-43-1Relevant academic research and scientific papers
Reactions of (Dichlorophosphinyl)methanesulfonyl Chloride
Fild, Manfred,Rieck, Hans-Peter
, p. 142 - 151 (2007/10/02)
Substitution of chlorine by fluorine in (dichlorophosphinyl)methanesulfonyl chloride (2) Cl2P(O)CH2SO2Cl leads to the fluorides F2P(O)CH2SO2X (X = Cl, F); their reactions leading to the fluorophosphorane F4PCH2SO2F and fluorophosphate anions of the type - and - (X = Cl, F) were investigated.Hydrolysis of 2 yields the acid (HO)2P(O)CH2SO2OH, from which esters and amides have been derived.The conversion of the esters to α,β-unsaturated sulfonic acid derivatives via the Horner-Wittig reaction is also described.
