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1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene is a complex organic chemical compound characterized by its unique structure with three phenyl rings, each substituted with trimethylsilyl and trifluoromethanesulfonyloxy functional groups. 1,3,5-TRIS[4-(TRIFLUOROMETHANESULFONYLOXY)-3-(TRIMETHYLSILYL)PHENYL]BENZENE is recognized for its high reactivity, making it a valuable asset in various chemical processes and industries.

847925-63-7

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847925-63-7 Usage

Uses

Used in Organic Synthesis:
1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene is used as a precursor in organic synthesis for its ability to facilitate the formation of new chemical compounds through its reactive functional groups.
Used in Chemical Reactions:
As a reagent, 1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene is utilized in various chemical reactions to promote specific transformations, taking advantage of its high reactivity.
Used in Pharmaceutical Industry:
1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene is employed in the pharmaceutical industry for its role in the synthesis of active pharmaceutical ingredients, contributing to the development of new drugs.
Used in Agrochemical Industry:
1,3,5-TRIS[4-(TRIFLUOROMETHANESULFONYLOXY)-3-(TRIMETHYLSILYL)PHENYL]BENZENE is also used in the agrochemical industry, where it may be involved in the synthesis of pesticides or other agrochemical products, leveraging its reactivity to create effective and targeted compounds.
Safety Considerations:
Due to its potentially hazardous nature, 1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene must be handled with care to ensure safety in laboratory and industrial settings. Proper safety protocols and equipment should be employed when working with 1,3,5-TRIS[4-(TRIFLUOROMETHANESULFONYLOXY)-3-(TRIMETHYLSILYL)PHENYL]BENZENE.

Check Digit Verification of cas no

The CAS Registry Mumber 847925-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,9,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 847925-63:
(8*8)+(7*4)+(6*7)+(5*9)+(4*2)+(3*5)+(2*6)+(1*3)=217
217 % 10 = 7
So 847925-63-7 is a valid CAS Registry Number.
InChI:InChI=1/C36H39F9O9S3Si3/c1-58(2,3)31-19-22(10-13-28(31)52-55(46,47)34(37,38)39)25-16-26(23-11-14-29(32(20-23)59(4,5)6)53-56(48,49)35(40,41)42)18-27(17-25)24-12-15-30(33(21-24)60(7,8)9)54-57(50,51)36(43,44)45/h10-21H,1-9H3

847925-63-7 Well-known Company Product Price

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  • TCI America

  • (T2467)  1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene  >92.0%(HPLC)

  • 847925-63-7

  • 1g

  • 1,690.00CNY

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847925-63-7SDS

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 1,3,5-Tris[4-(trifluoromethanesulfonyloxy)-3-(trimethylsilyl)phenyl]benzene

1.2 Other means of identification

Product number -
Other names [4-[3,5-bis[4-(trifluoromethylsulfonyloxy)-3-trimethylsilylphenyl]phenyl]-2-trimethylsilylphenyl] trifluoromethanesulfonate

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:847925-63-7 SDS

847925-63-7Downstream Products

847925-63-7Relevant academic research and scientific papers

Facile synthesis of polycyclic aromatic hydrocarbons via a trisaryne equivalent

Ikadai, Junnai,Yoshida, Hiroto,Ohshita, Joji,Kunai, Atsutaka

, p. 56 - 57 (2005)

1,3,5-Tris[4-trifluoromethanesulfonyloxy-3-(trimethylsilyl)-phenyl]benzene (1), a trisaryne equivalent, was synthesized. The Diels-Alder reaction or the palladium-catalyzed hexasilylation by use of 1 gave modest to excellent yields of diverse polyaromatic

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