1708-73-2 Usage
Description
[(Chloromethyl)sulfanyl]ethane, also known as (Chloromethyl)thio-ethane, is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds. It is characterized by its chloromethyl and sulfanyl functional groups, which contribute to its reactivity and potential applications in chemical synthesis.
Uses
Used in Chemical Synthesis:
[(Chloromethyl)sulfanyl]ethane is used as an intermediate in the synthesis of Phorate Oxon Sulfone (P353515) for its role in creating essential chemical structures. Phorate Oxon Sulfone is a major metabolite of Phorate (P353500), which functions as an inhibitor of acetylcholinesterase and pseudocholinesterase, playing a significant role in the development of pesticides and other agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(chloromethyl)sulfanyl]ethane can be utilized as a building block for the development of new drugs targeting acetylcholinesterase and pseudocholinesterase enzymes. Its unique functional groups can be exploited to create novel drug candidates with improved efficacy and selectivity.
Used in Agrochemical Industry:
[(Chloromethyl)sulfanyl]ethane is used as a key intermediate in the production of Phorate Oxon Sulfone, which is derived from Phorate, a widely used insecticide. This application highlights its importance in the development of more effective and environmentally friendly pest control solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 1708-73-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,0 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1708-73:
(6*1)+(5*7)+(4*0)+(3*8)+(2*7)+(1*3)=82
82 % 10 = 2
So 1708-73-2 is a valid CAS Registry Number.
1708-73-2Relevant articles and documents
Regiochemistry and reactivity in the chlorination of sulfides
Hancock, James Reid,Hardstaff, William Rayne,Johns, Paul Alan,Langler, Richard Francis,Mantle, William Stanley
, p. 1472 - 1480 (2007/10/02)
Huheey's original method for the calculation of substituent electronegativities is modified so that isomeric groups have different electronegativities.The modified form of Huheey's method is then employed to show that our previously published method for anticipating regiochemistry in asymmetric sulfide chlorination, i.e., ΔXP calculations for the α and α' substituents in the sulfide substrates, is successful in all fifty known cases.A new reactivity function (RP) is defined, for the sulfenium ion intermediates, which permits one to anticipate when substrates become inert to chlorine in exhaustive chlorinations conducted in aprotic media.
