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947725-04-4

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  • factory supply 4-tert-Butyl-2,6-dimethylphenylsulphur trifluoride, 90% CAS:947725-04-4 CAS NO.947725-04-4

    Cas No: 947725-04-4

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947725-04-4 Usage

Chemical Properties

White powder

Uses

Different sources of media describe the Uses of 947725-04-4 differently. You can refer to the following data:
1. Air and thermally stable alternative to DAST. Efficient deoxofluorinating agent for a wide variety of substrates.
2. Features:Tolerance of many functional groupsHighly selective functionalizationHighly efficient and broad reaction scopeMild reaction conditionsGenerally superior reactivity and selectivity to SF4 and easier and safer to handle.Shown to promote nucleophilic deoxofluorination reactions and exhibits excellent thermal stability, up to 150 °C, therefore rendering it safely applicable in a variety of processes, including industrial scale production.Novel fluorinating reagent applicable to a variety of chemical processes (Scheme 1).Refer to the Datasheet for more information on Fluolead?: A Novel New Versatile Fluorinating Agent
3. 4-tert-Butyl-2,6-dimethylphenylsulfur Trifluoride is a deoxofluorination reagent used in an improved method of synthesis of arylsulfur trifluorides.

General Description

4-tert-Butyl-2,6-dimethylphenylsulfur trifluoride is a thermally stable, easy-to-handle, versatile deoxofluorinating agent that also shows high stability on contact with water. It is a superior alternative to diethylaminosulfur trifluoride (DAST).

Check Digit Verification of cas no

The CAS Registry Mumber 947725-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,7,2 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 947725-04:
(8*9)+(7*4)+(6*7)+(5*7)+(4*2)+(3*5)+(2*0)+(1*4)=204
204 % 10 = 4
So 947725-04-4 is a valid CAS Registry Number.

947725-04-4 Well-known Company Product Price

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  • TCI America

  • (B3664)  4-tert-Butyl-2,6-dimethylphenylsulfur Trifluoride  >90.0%(T)

  • 947725-04-4

  • 1g

  • 550.00CNY

  • Detail
  • TCI America

  • (B3664)  4-tert-Butyl-2,6-dimethylphenylsulfur Trifluoride  >90.0%(T)

  • 947725-04-4

  • 5g

  • 1,190.00CNY

  • Detail
  • Aldrich

  • (734039)  4-tert-Butyl-2,6-dimethylphenylsulfur trifluoride  

  • 947725-04-4

  • 734039-1G

  • 563.94CNY

  • Detail
  • Aldrich

  • (734039)  4-tert-Butyl-2,6-dimethylphenylsulfur trifluoride  

  • 947725-04-4

  • 734039-5G

  • 1,629.81CNY

  • Detail
  • Aldrich

  • (734039)  4-tert-Butyl-2,6-dimethylphenylsulfur trifluoride  

  • 947725-04-4

  • 734039-25G

  • 4,403.88CNY

  • Detail

947725-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-tert-butyl-2,6-dimethylphenyl)-trifluoro-λ<sup>4</sup>-sulfane

1.2 Other means of identification

Product number -
Other names Fluolead

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:947725-04-4 SDS

947725-04-4Relevant articles and documents

Method of Synthesis of Arylsulfur Trifluorides and Use as in situ Deoxofluorination Reagent

-

Page/Page column 2, (2012/04/11)

The invention is a method of synthesizing Arylsulfur Trifluorides, such as Fluolead, by reacting BR2 and KF (or suitable alkali metal fluoride) in acetonitrile (or other suitable solvent). The invention also comprises using the Fluolead (or its

SUBSTITUTED PHENYLSULFUR TRIFLUORIDE AND OTHER LIKE FLUORINATING AGENTS

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Page/Page column 12, (2008/06/13)

Novel substituted phenylsulfur trifluorides that act as fluorinating agents are disclosed. Also disclosed are methods for their preparation and methods for their use in introducing one or more fluorine atoms into target substrate compounds.

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