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18546-89-9

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18546-89-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18546-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,4 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18546-89:
(7*1)+(6*8)+(5*5)+(4*4)+(3*6)+(2*8)+(1*9)=139
139 % 10 = 9
So 18546-89-9 is a valid CAS Registry Number.

18546-89-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-[4-[(4-trimethylsilylphenyl)disulfanyl]phenyl]silane

1.2 Other means of identification

Product number -
Other names RNHDNEGPJOGBBX-UHFFFAOYSA

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:18546-89-9 SDS

18546-89-9Relevant articles and documents

Ipso-Fluorination of aryltrimethylsilanes using xenon difluoride

Lothian, Aileen P.,Ramsden, Christopher A.,Shaw, Maxine M.,Smith, Rachel G.

experimental part, p. 2788 - 2793 (2011/05/02)

Reaction of aryltrimethylsilanes with xenon difluoride in C 6F6/Pyrex at room temperature gives aryl fluorides in good yield. The reaction is inhibited when acetonitrile is used as solvent but proceeds well in CFCl3/Pyrex or CH 2Cl2/Pyrex. Pyrex appears to be a very effective heterogeneous catalyst for this ipso-fluorination. The reaction does not proceed in PTFE, quartz, soda glass or glassy-carbon flasks or Pyrex flasks pre-rinsed with 2 M NaOH. Aryltrimethylstannanes and arylboronic acids and their esters do not undergo ipso-fluorination under similar conditions. Plausible mechanisms involving electrophilic addition of polarised xenon difluoride [FXeδ+?F→Pyrex δ-] followed by ligand coupling are discussed.

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