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Tributyl(fluoro)silane, also known as fluorotri-n-butylsilane, is an organosilicon compound with the chemical formula (C4H9)3SiF. It is a colorless, volatile liquid that is sensitive to air and moisture. tributyl(fluoro)silane is primarily used as a silylating agent in organic synthesis, particularly for the protection of alcohols and carboxylic acids. It can also be used as a fluorinating agent in various chemical reactions. Due to its reactivity, tributyl(fluoro)silane is typically handled under an inert atmosphere and stored away from heat and light.

338-49-8

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338-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 338-49-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 338-49:
(5*3)+(4*3)+(3*8)+(2*4)+(1*9)=68
68 % 10 = 8
So 338-49-8 is a valid CAS Registry Number.

338-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name tributyl(fluoro)silane

1.2 Other means of identification

Product number -
Other names tributylfluorosilane

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:338-49-8 SDS

338-49-8Downstream Products

338-49-8Relevant academic research and scientific papers

Rhodium-catalyzed synthesis of diaryl sulfides using aryl fluorides and sulfur/organopolysulfides

Arisawa, Mieko,Ichikawa, Takuya,Yamaguchi, Masahiko

supporting information, p. 5318 - 5321 (2013/01/15)

Substituted pentafluorobenzenes react with sulfur to give bis(4-substituted 2,3,5,6-tetrafluorophenyl) sulfides in the presence of RhH(PPh 3)4, 1,2-bis(diphenylphosphino)benzene (dppBz), and tributylsilane. The reaction proceeds efficiently between room temperature and 80 °C. A comparative study of the reactivities of an organic trisulfide and a tetrasulfide showed notable substrate specificity. Di-tert-butyl tetrasulfide reacted with reactive aryl monofluorides and substituted pentafluorobenzenes. Di-tert-butyl trisulfide reacted with aryl monofluorides. The reactivity was explained on the basis of the difference in S-S bond energy.

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