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5721-88-0

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5721-88-0 Usage

General Description

1-(1,3-Oxathiolane-2-yl)benzene, also known as o-xylene-2-thiol, is a chemical compound consisting of a benzene ring attached to a 1,3-oxathiolane moiety. 1-(1,3-Oxathiolane-2-yl)benzene is used primarily in the production of various types of polymers, resins, and other industrial materials. It is also employed as a precursor in the synthesis of pharmaceuticals and agrochemicals. O-xylene-2-thiol has a strong odor and is classified as a hazardous chemical, requiring proper handling and storage to prevent harmful exposure. Its chemical properties and reactivity make it a valuable building block for a range of chemical products and processes in the manufacturing industry.

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

5721-88-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,3-oxathiolane

1.2 Other means of identification

Product number -
Other names 2-phenyl-1,3-oxathiolate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5721-88-0 SDS

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.

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