49592-61-2 Usage
Uses
Used in Pharmaceutical Industry:
3-Chloro-4-hydroxytetrahydrothiophene-1,1-dioxide is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure allows it to be a key component in the development of new medications, particularly those targeting bacterial and fungal infections.
Used in Agrochemical Industry:
In the agrochemical sector, 3-chloro-4-hydroxytetrahydrothiophene-1,1-dioxide is utilized as an active ingredient in the formulation of pesticides and fungicides. Its demonstrated antibacterial and antifungal properties make it a valuable asset in protecting crops from diseases and pests.
Used in Materials Science:
3-Chloro-4-hydroxytetrahydrothiophene-1,1-dioxide is employed as a component in the development of new materials with specific properties. Its chemical structure contributes to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity, depending on the application.
Used in Antimicrobial Applications:
3-Chloro-4-hydroxytetrahydrothiophene-1,1-dioxide is used as an antimicrobial agent for its potential to combat bacterial and fungal infections. Its unique structure allows it to target and inhibit the growth of various pathogens, making it a promising candidate for use in medical and industrial settings to prevent the spread of infections.
Check Digit Verification of cas no
The CAS Registry Mumber 49592-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,9 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 49592-61:
(7*4)+(6*9)+(5*5)+(4*9)+(3*2)+(2*6)+(1*1)=162
162 % 10 = 2
So 49592-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H7ClO3S/c5-3-1-9(7,8)2-4(3)6/h3-4,6H,1-2H2
49592-61-2Relevant academic research and scientific papers
Oxygen-17 Nuclear Magnetic Resonance Spectral Investigation of 3-Alkoxy-trans-3,4-Disubstituted-Thiolane 1,1-Dioxides and Related Compounds
Sammakia, Tarek H.,Harris, David L.,Evans, Slayton A.
, p. 747 - 752 (2007/10/02)
The (17)O NMR spectra of 3-alkoxythiolane 1,1-dioxides indicate that the sulfonyl oxygens are diastereotopic but their chemical shift differences are essentially independent of the structure of the alkyl group in the alkoxy moiety.Eu(fod)3 enhances the (17)O chemical shift difference between the diastereotopic sulfonyl oxygens in 3-isopropoxythiolane 1,1-dioxide and shifts both oxygens upfield. α,β-Unsaturation deshields the sulfonyl oxygens in both five- and six-membered rings.
REACTION OF SOLFOLENE OXIDES WITH ACYL CHLORIDES AND CHLORO ETHERS
Mukhamedova, L. A.,Kursheva, L. I.,Khasyanzyanova, F. S.
, p. 707 - 710 (2007/10/02)
The reaction of sulfolene and 3-methylsulfolene oxides with acetyl chloride, benzoyl chloride, and chlorodimethyl and chloromethyl ethyl ethers was studied.It is shown that sulfolene oxides are rather stable in acidic media and undergo ring opening only w
