Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1469-73-4

Post Buying Request

1469-73-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1469-73-4 Usage

Description

4-Methyl-1,3,2-dioxathiolane 2-oxide is an organic compound with the molecular formula C5H10O3S. It is a colorless to pale yellow liquid and is a mixture of isomers. This product has been enhanced for energy efficiency.

Uses

Used in Chemical Synthesis:
4-Methyl-1,3,2-dioxathiolane 2-oxide is used as a reagent in the preparation of deep eutectic solvents for SO2 cycloaddition reactions. These reactions are important in the synthesis of various organic compounds and materials.
Used in Energy Storage:
In the energy storage industry, 4-methyl-1,3,2-dioxathiolane 2-oxide is used as a film-forming electrolyte additive for lithium-ion battery electrolytes. Its application enhances the performance and stability of the batteries, contributing to improved energy efficiency.
Used in Advanced Battery Technologies:
4-Methyl-1,3,2-dioxathiolane 2-oxide is also utilized as a solvent for making non-aqueous electrolytes for lithium-ion and lithium-sulfur batteries. This application is crucial for the development of advanced battery technologies that require high energy density and improved safety features.

Check Digit Verification of cas no

The CAS Registry Mumber 1469-73-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,6 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1469-73:
(6*1)+(5*4)+(4*6)+(3*9)+(2*7)+(1*3)=94
94 % 10 = 4
So 1469-73-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H6O3S/c1-3-2-5-7(4)6-3/h3H,2H2,1H3

1469-73-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (M2471)  4-Methyl-1,3,2-dioxathiolane 2-Oxide (mixture of isomers)  >98.0%(GC)

  • 1469-73-4

  • 5g

  • 300.00CNY

  • Detail
  • TCI America

  • (M2471)  4-Methyl-1,3,2-dioxathiolane 2-Oxide (mixture of isomers)  >98.0%(GC)

  • 1469-73-4

  • 25g

  • 980.00CNY

  • Detail
  • Aldrich

  • (774456)  1,2-Propyleneglycol sulfite Green Alternative  ≥98%

  • 1469-73-4

  • 774456-10G

  • 1,045.98CNY

  • Detail

1469-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-1,3,2-dioxathiolane 2-oxide

1.2 Other means of identification

Product number -
Other names 4-methylethylene sulphite

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:1469-73-4 SDS

1469-73-4Relevant articles and documents

A method for preparing [...] (by machine translation)

-

Paragraph 0023-0026; 0031; 0033-0034; 0039; 0041-0042, (2019/05/29)

The invention relates to a method for preparing [...], comprising the following steps: S1. The nucleophilic substitution reaction: to propylene glycol and thionyl chloride as the starting material, chloroform as solvent, the nucleophilic substitution reaction, by the sulfurous acid propylene chloroform solution; S2. Oxidation reaction: high iodic acid as the oxidizing agent, the ruthenium trichloride hydrate catalyst, to S1 to obtain solution in the oxidation process is performed on the sulfurous acid propylene shall [...]; S3. The refined purification: sulfuric acid propylene crude soluble in chloroform, under the protection of nitrogen, heating to reflux is fully dissolved, then lower the temperature crystallization, filtering, filters the cake to pass through reduced-pressure drying, to obtain. The mild reaction conditions of the present invention, the synthetic process is simple, easy to operate, high safety, preparation cycle is short, the raw materials used are simple and easy to obtain, the cost is low, few by-products, the preparation of the product has high purity, low water content, low acid value of the product, the product yield is high, and is suitable for industrial production. (by machine translation)

Synthesis of cyclic sulfites from epoxides and sulfur dioxide with silica-immobilized homogeneous catalysts

Takenaka, Yasumasa,Kiyosu, Takahiro,Mori, Goro,Choi, Jun-Chul,Fukaya, Norihisa,Sakakura, Toshiyasu,Yasuda, Hiroyuki

experimental part, p. 194 - 199 (2012/06/30)

Quaternary ammonium- and amino-functionalized silica catalysts have been prepared for the selective synthesis of cyclic sulfites from epoxides and sulfur dioxide, demonstrating the effects of immobilizing the homogeneous catalysts on silica. The cycloaddition of sulfur dioxide to various epoxides was conducted under solvent-free conditions at 100 °C. The quaternary ammonium- and amino-functionalized silica catalysts produced cyclic sulfites in high yields (79-96 %) that are comparable to those produced by the homogeneous catalysts. The functionalized silica catalysts could be separated from the product solution by filtration, thereby avoiding the catalytic decomposition of the cyclic sulfite products upon distillation of the product solution. Heterogenization of a homogeneous catalyst by immobilization can, therefore, improve the efficiency of the purification of crude reaction products. Despite a decrease in catalytic activity after each recycling step, the heterogeneous pyridine-functionalized silica catalyst provided high yields after as many as five recycling processes. Immobilized for crimes of pyrolysis: Quaternary ammonium- and amino-functionalized silica catalysts promote the cycloaddition of sulfur dioxide to epoxides to produce cyclic sulfites in high yields (79-96 %) that are comparable to those with the homogeneous catalysts. Separation of the functionalized silica catalyst from the product solution by filtration avoids pyrolysis of the cyclic sulfites during purification by distillation. Copyright

Synthesis of hydroxy sulfonate surfactants

Rist, ystein,Carlsen, Per H. J.

, p. 1169 - 1178 (2007/10/03)

The selective synthesis of sulfonate surfactants with side chains containing ether- and hydroxy groups was carried out using cyclic sulfates as epoxide analogues. The main chain was elaborated from 1,2-dodecane sulfate by the addition of various hydroxy/alkoxysulfonates. Ethyleneoxy- and 1,2-propyleneoxy- groups were introduced using ethylene sulfate and 1,2-propylene sulfate, respectively.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1469-73-4