5721-88-0 Usage
Description
1-(1,3-Oxathiolane-2-yl)benzene, also known as o-xylene-2-thiol, is a chemical compound that features a benzene ring with a 1,3-oxathiolane group attached to it. 1-(1,3-Oxathiolane-2-yl)benzene is recognized for its strong odor and is classified as a hazardous chemical, necessitating careful handling and storage to avoid harmful exposure. Its unique chemical properties and reactivity render it a versatile building block in the manufacturing industry, particularly for creating a variety of polymers, resins, and other industrial materials. Furthermore, it serves as a crucial precursor in the synthesis of pharmaceuticals and agrochemicals, highlighting its importance in both the chemical and healthcare sectors.
Uses
Used in Chemical Manufacturing:
1-(1,3-Oxathiolane-2-yl)benzene is used as a building block for the production of various polymers and resins, contributing to the structural integrity and performance of these materials. Its application in this industry is due to its ability to form stable and functional polymers with desirable properties.
Used in Pharmaceutical Synthesis:
As a precursor, 1-(1,3-Oxathiolane-2-yl)benzene is utilized in the synthesis of pharmaceuticals. Its role in this application stems from its reactivity and compatibility with other chemical compounds, enabling the creation of new and effective medications.
Used in Agrochemical Production:
1-(1,3-Oxathiolane-2-yl)benzene is also employed as a starting material in the production of agrochemicals. Its use in this industry is attributed to its potential to form compounds with pesticidal, herbicidal, or fungicidal properties, thereby contributing to agricultural productivity and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 5721-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5721-88:
(6*5)+(5*7)+(4*2)+(3*1)+(2*8)+(1*8)=100
100 % 10 = 0
So 5721-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H10OS/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-5,9H,6-7H2
5721-88-0Relevant articles and documents
Blue LED-Promoted Oxathiacetalization of Aldehydes and Ketones
Liu, You-Chen,Reddy, Daggula Mallikarjuna,Chen, Xin-An,Shieh, Yi-Chen,Lee, Chin-Fa
, p. 2542 - 2552 (2020/04/27)
In synthetic chemistry, the protection of aldehydes and ketones is crucial during multistep synthesis of complex molecules. Organic chemists have paid substantial attention to the synthesis of 1,3-oxathiolanes and 1,3-oxathianes because of their considera
Silica-gel supported sulfamic acid (SA/SiO2) as an efficient and reusable catalyst for conversion of ketones into oxathioacetals and dithioacetals
Aoyama, Tadashi,Suzuki, Toshihiko,Nagaoka, Takashi,Takido, Toshio,Kodomari, Mitsuo
, p. 553 - 566 (2013/01/15)
A simple and efficient method for the conversion of carbonyl compounds to oxathioacetals and dithioacetals using SA/SiO2 as an acid catalyst has been achieved. SA/SiO2 is easily recovered from the reaction mixture and can be reused at least 15 times without loss of catalytic activity.
An efficient method for the oxathioacetalization of carbonyl compounds using N-bromosaccharin as a catalyst
Alinezhad, Heshmatollah,Fallahi, Shahrouz
experimental part, p. 927 - 929 (2012/08/28)
A mild and highly chemoselective method for the preparation of oxathiolane from aliphatic and aromatic aldehydes and ketones with 2-mercaptoethanol in the presence of catalytic amount of N-bromosaccharin at room temperature is reported.
