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4-TOLYL-N-FLUORO-N-METHYLSULPHONAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88303-12-2

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88303-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88303-12-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,0 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88303-12:
(7*8)+(6*8)+(5*3)+(4*0)+(3*3)+(2*1)+(1*2)=132
132 % 10 = 2
So 88303-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H10FNO2S/c1-7-3-5-8(6-4-7)13(11,12)10(2)9/h3-6H,1-2H3

88303-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-fluoro-N,4-dimethylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-methyl-N-fluoro-p-toluenesulfonamide

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:88303-12-2 SDS

88303-12-2Relevant academic research and scientific papers

Transition-Metal-Free α Csp3?H Cyanation of Sulfonamides

Zhou, Liejin,Wei, Siqi,Lei, Ziran,Zhu, Gangguo,Zhang, Zuxiao

supporting information, p. 7103 - 7107 (2021/04/16)

This report describes the site-selective α-functionalization of sulfonylamide derivatives through the in-situ generation of imine intermediates. The N?F sulfonylamides, which could facilitate the elimination to generate imines, are coupled with TBACN to e

Fluorination of carbanions with N-fluoro-N-alkylsulfonamides

-

, (2008/06/13)

Process for fluorinating an organic carbanion, which process comprises contacting and reacting, in a dry inert atmosphere, the compound of the formula selected from STR1 wherein STR2 is the carbanion, M is a counter ion, and X is a halide and a selected N-flouro-N-alkylsulfonamide.

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