24588-75-8 Usage
Description
2-[4-(Dimethylamino)phenyl]-1,3-dithiane is a dithiane derivative with the molecular formula C12H17NS. It features a phenyl group substituted with a dimethylamino group, making it a versatile chemical compound in the field of organic synthesis.
Uses
Used in Organic Synthesis:
2-[4-(Dimethylamino)phenyl]-1,3-dithiane is used as a reagent for the introduction of the dithiane functional group into organic molecules. Its ability to protect carbonyl groups makes it a valuable component in various organic synthesis processes.
Used in Pharmaceutical Compound Preparation:
2-[4-(Dimethylamino)phenyl]-1,3-dithiane is utilized in the preparation of different pharmaceutical compounds, contributing to the development of new drugs and therapeutic agents.
Used in Anti-Inflammatory Applications:
2-[4-(Dimethylamino)phenyl]-1,3-dithiane has been studied for its potential as an anti-inflammatory agent, which could be beneficial in treating conditions characterized by inflammation.
Used in Anti-Cancer Applications:
Research has also explored the compound's potential as an anti-cancer agent, indicating its possible role in the development of new cancer treatments.
Used in Material and Technology Development:
Furthermore, 2-[4-(Dimethylamino)phenyl]-1,3-dithiane has been considered for its potential use in the development of new materials and technologies, showcasing its broad applicability across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 24588-75-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24588-75:
(7*2)+(6*4)+(5*5)+(4*8)+(3*8)+(2*7)+(1*5)=138
138 % 10 = 8
So 24588-75-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NS2/c1-13(2)11-6-4-10(5-7-11)12-14-8-3-9-15-12/h4-7,12H,3,8-9H2,1-2H3
24588-75-8Relevant articles and documents
PhIO-Mediated oxidative dethioacetalization/dethioketalization under water-free conditions
Du, Yunfei,Ouyang, Yaxin,Wang, Xi,Wang, Xiaofan,Yu, Zhenyang,Zhao, Bingyue,Zhao, Kang
, p. 48 - 65 (2021/06/16)
Treatment of thioacetals and thioketals with iodosobenzene in anhydrous DCM conveniently afforded the corresponding carbonyl compounds in high yields under water-free conditions. The mechanistic studies indicate that this dethioacetalization/dethioketalization process does not need water and the oxygen of the carbonyl products comes from the hypervalent iodine reagent.
Mesoporous sBa-15 silica catalyst functionalized with phenylsulfonic acid groups (SbA-15-ph-So3h) as efficient nanocatalyst for chemoselective thioacetalization of carbonyl compounds
Sedrpoushan, Alireza,Ghazizadeh, Habibollah
, p. 112 - 118 (2017/01/18)
In this research a Nano acidic catalyst was prepared and its efficiency on thioacetalization of carbonyl compounds was examined. For this aim we used modified SBA-15 as support, which have been modified by phenolic and sulfonic acid. SBA-15 is a member of
Silica-supported phosphorus pentoxide: A reusable catalyst for S,S-acetalization of carbonyl groups under ambient conditions
Shaterian, Hamid Reza,Azizi, Kobra,Fahimi, Nafiseh
experimental part, p. 85 - 91 (2012/01/06)
Phosphorus pentoxide supported on silica gel (P2O 5/SiO2) efficiently acts as a highly active and reusable catalyst for cyclic and non-cyclic S,S-acetalization of a variety of carbonyl compounds under mild, solvent-free an
