3643-97-8 Usage
Uses
Used in Pharmaceutical Industry:
6-methyl-2,3-dihydro-1,4-oxathiine is used as a building block for the synthesis of various biologically active compounds due to its unique sulfur-containing heterocyclic structure.
Used in Organic Synthesis Industry:
6-methyl-2,3-dihydro-1,4-oxathiine is utilized as an intermediate in the synthesis of complex organic molecules, taking advantage of its reactive thioether functional group.
Used in Antimicrobial Applications:
6-methyl-2,3-dihydro-1,4-oxathiine has been studied for its potential antimicrobial properties, making it a candidate for development as an antimicrobial agent in various applications.
Used in Anti-inflammatory Applications:
6-methyl-2,3-dihydro-1,4-oxathiine has also been investigated for its anti-inflammatory effects, suggesting a possible use in the development of anti-inflammatory medications or treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 3643-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3643-97:
(6*3)+(5*6)+(4*4)+(3*3)+(2*9)+(1*7)=98
98 % 10 = 8
So 3643-97-8 is a valid CAS Registry Number.
3643-97-8Relevant academic research and scientific papers
Studies on the Preparation of Dihydro-1,4-oxathiines. Computer-Assisted Evaluation of the Results of Retrosynthetic Analysis Verified by Synthetic Experiments and By-Product Analyses. Synthetic Pathways Involving α-Sulfenylated Ketones and 1,3-Oxathiolanes of α-Halo and α-Hydroxy K...
Nevalainen, Vesa,Pohjala, Esko,Maelkoenen, Pentti,Hukkanen, Heikki
, p. 591 - 602 (2007/10/02)
The preparation of 2- and 2,3-substituted 5,6-dihydro-1,4-oxathiines has been studied by computer simulation and by experiment.Three major synthetic pathways, involving 2-(1-hydroxyalkyl)-1,3-oxathiolanes, 2-(1-haloalkyl)-1,3-oxathiolanes, 2-hydroxyethylthiomethyl ketones, methanesulfonates of 2-hydroxyethylthiomethyl ketones and 2-choroethylthiomethyl ketones as intermediates, were evaluated, by running the program CAMEO, and by experiment.The results of the two approaches were compared and the major by-products of the reactions were identified by GLC/MS.
