62217-35-0 Usage
Description
Dimethyl 1,3-Benzodithiol-2-ylphosphonate is a phosphonate ester with the molecular formula C6H7O2PS2, featuring a benzodithiol group that imparts unique chemical properties to the compound. It is utilized in various applications across different industries due to its versatility and reactivity.
Uses
Used in Organic Synthesis:
Dimethyl 1,3-Benzodithiol-2-ylphosphonate is used as a reagent in organic synthesis for its ability to facilitate the formation of complex organic molecules. Its unique structure allows it to participate in various chemical reactions, making it a valuable component in the synthesis of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Dimethyl 1,3-Benzodithiol-2-ylphosphonate is used as a building block for the production of various drugs. Its chemical properties enable it to be incorporated into the molecular structures of medications, contributing to their therapeutic effects.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, this compound is used as a building block for the development of crop protection agents and other agricultural products. Its reactivity and stability make it suitable for creating effective and long-lasting agrochemicals.
Used in Plastics and Polymers Industry:
Dimethyl 1,3-Benzodithiol-2-ylphosphonate is used as a stabilizer and flame retardant in the production of plastics and polymers. Its presence in these materials helps to improve their resistance to heat and fire, enhancing their safety and durability.
Safety Precautions:
It is crucial to handle Dimethyl 1,3-Benzodithiol-2-ylphosphonate with care, as it can be toxic and harmful if not used properly. Adequate safety measures should be taken to minimize exposure and ensure the safe use of this compound in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62217-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,1 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62217-35:
(7*6)+(6*2)+(5*2)+(4*1)+(3*7)+(2*3)+(1*5)=100
100 % 10 = 0
So 62217-35-0 is a valid CAS Registry Number.
62217-35-0Relevant articles and documents
Synthesis of new functionalized compounds related to π-extended tetrathiafulvalenes with quinonoidal structures bearing a ferrocene moiety
Sarhan, Abd El-Wareth A. O.,Murakami, Makoto,Izumi, Taeko
, p. 1055 - 1066 (2002)
A number of π-extended conjugated tetrathiafulvalene (TTF) analogues were synthesized as new π-donors, and their structures and physical properties were determined. UV/Vis spectra and cyclic voltammetry of the π-extended ferrocenyl donors were studied in comparison with ferrocene, ferrocenylquinone, and the parent donor. A three-electron redox behaviour was observed. The absorption spectrum of the new donor 16 showed a slight red-shift and a slight increase in intensity relative to the compared compounds.
Synthesis and photochromic behaviour of new dipyrrolylperfluorocyclopentenes
Heynderickx, Arnault,Kaou, Ali Mohamed,Moustrou, Corinne,Samat, Andre,Guglielmetti, Robert
, p. 1425 - 1432 (2007/10/03)
The synthesis of new photoswitchable dipyrrolylethenes having different π-conjugated chain lengths, employing Wittig-Horner reaction, Knoevenagel condensation, Suzuki palladium catalyzed cross-coupling or Sonogashira coupling, is reported. Their photochemical behaviour, and in particular, their thermal stability has been investigated upon continuous irradiation with light of appropriate wavelengths.
