53811-23-7 Usage
Dithiane derivative
A type of organic compound 2-(phenylsulfanyl)-1,3-dithiane is a derivative of dithiane, which is a saturated six-membered ring containing two sulfur atoms and two carbon atoms.
Synthetic building block
Used in organic chemistry 2-(phenylsulfanyl)-1,3-dithiane is commonly used as a synthetic building block in organic chemistry, particularly for the synthesis of complex organic molecules.
Applications
Pharmaceutical, agrochemical, and materials science 2-(phenylsulfanyl)-1,3-dithiane has been utilized in the preparation of various pharmaceuticals, agrochemicals, and materials science applications.
Protecting carbonyl groups
In synthesis of natural products and bioactive compounds The compound is known for its ability to protect carbonyl groups, which has been employed in the synthesis of natural products and other bioactive compounds.
Antimicrobial and antifungal properties
Potential applications 2-(phenylsulfanyl)-1,3-dithiane has been investigated for its potential antimicrobial and antifungal properties, indicating possible applications in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 53811-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,1 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53811-23:
(7*5)+(6*3)+(5*8)+(4*1)+(3*1)+(2*2)+(1*3)=107
107 % 10 = 7
So 53811-23-7 is a valid CAS Registry Number.
53811-23-7Relevant academic research and scientific papers
Enantioselective preparation of 2-substituted-1,3-dithiane 1-oxides using modified Sharpless sulphoxidation procedures
Page, Philip C. Bulman,Wilkes, Robin D.,Namwindwa, Ernest S.,Witty, Michael J.
, p. 2125 - 2154 (2007/10/03)
Enantioselective sulphoxidation of a wide range of 2-substituted-1,3-diathianes has been carried out using modified Sharpless conditions to furnish the corresponding sulphoxides in optically enriched form. Deacylation of 2-acyl-1,3-dithiane 1-oxide deriva
STUDY OF THE ANOMERIC EFFECT IN 2-SUBSTITUTED 1,3-DITHIANES
Juaristi, Eusebio,Tapia, Josefina,Mendez, Rodolfo
, p. 1253 - 1264 (2007/10/02)
The conformational analysis of several 2-substituted 1,3-dithianes made possible the evaluation of S-C-Y anomeric interactions, where Y=SCH3,SC6H5,CO2CH3,COC6H5,CO2H and N(CH3)2.The relative magnitude of the effects observed for these groups odithiane(Y)-ΔGocyclohexane(Y)> can be explained in terms of the combined influence of dipole/dipole and two-electron stabilizing interactions (stereoelectronic effect).
