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Methyl(oxolan-2-ylmethyl) sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15396-31-3

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15396-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15396-31-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,9 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 15396-31:
(7*1)+(6*5)+(5*3)+(4*9)+(3*6)+(2*3)+(1*1)=113
113 % 10 = 3
So 15396-31-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O3S/c1-10(7,8)5-6-3-2-4-9-6/h6H,2-5H2,1H3

15396-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(methylsulfonylmethyl)oxolane

1.2 Other means of identification

Product number -
Other names Methyl tetrahydrofurfuryl sulfone

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:15396-31-3 SDS

15396-31-3Downstream Products

15396-31-3Relevant academic research and scientific papers

General sulfone construction: Via sulfur dioxide surrogate control

Chen, Shihao,Li, Yaping,Wang, Ming,Jiang, Xuefeng

supporting information, p. 322 - 326 (2020/02/13)

A highly efficient one-step synthesis of alkyl-alkyl and aryl-alkyl sulfones with a facile combination of halides, sulfur dioxide surrogates and phosphate esters is described. When thiourea dioxide was employed as a reductive sulfur dioxide surrogate, alkyl-alkyl sulfones were obtained under transition metal free conditions. Aryl-alkyl sulfones were obtained with an extremely low catalytic loading (0.2 mol%) via altering the mask of sulfur dioxide surrogates to sodium dithionite. A phosphate ester was employed as a stable and readily available alkyl source. Notably, this protocol has been applied to the late-stage modification of natural products and bioactive molecules.

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