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1-(tri-n-butylstannyl)-2-fluorobenzene is an organotin compound characterized by the presence of a tri-n-butyltin group attached to a fluorobenzene molecule. 1-(tri-n-butylstannyl)-2-fluorobenzene is a colorless liquid with a molecular formula of C16H27FSn and a molecular weight of 343.07 g/mol. It is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Stille coupling reaction, a widely employed cross-coupling method in organic chemistry. The compound's structure features a fluorine atom at the 2-position of the benzene ring and a tri-n-butyltin group at the 1-position, which provides unique reactivity and selectivity in various chemical transformations. Due to its potential toxicity and environmental impact, handling and disposal of 1-(tri-n-butylstannyl)-2-fluorobenzene should be done with proper safety precautions and in accordance with local regulations.

7579-74-0

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7579-74-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7579-74-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7579-74:
(6*7)+(5*5)+(4*7)+(3*9)+(2*7)+(1*4)=140
140 % 10 = 0
So 7579-74-0 is a valid CAS Registry Number.

7579-74-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-fluoro-2-(tributylstannyl)benzene

1.2 Other means of identification

Product number -
Other names 1-(tri-n-butylstannyl)-2-fluorobenzene

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:7579-74-0 SDS

7579-74-0Relevant academic research and scientific papers

Synchronous Ar-F and Ar-Sn bond formation through fluorostannylation of arynes

Yoshida, Hiroto,Yoshida, Ryuma,Takaki, Ken

, p. 8629 - 8632 (2013)

An aryne insertion into the F-Sn bond of tributyltin fluoride leads to the synchronous formation of Ar-F and Ar-Sn bonds to afford diverse 2-fluoroarylstannanes straightforwardly. The formal total synthesis of flurbiprofen by using a fluorostannylation product is also reported. Copyright

A Sn atom-economical approach toward arylstannanes: Ni-catalysed stannylation of aryl halides using Bu3SnOMe

Komeyama, Kimihiro,Asakura, Ryota,Takaki, Ken

supporting information, p. 8713 - 8716 (2015/08/24)

Stannylation of carbon-halogen bonds is one of the most promising and straightforward approaches for the preparation of organostannane compounds. Although a wide variety of methods are now available, all protocols require the use of highly nucleophilic organometals or wasteful stannyl sources like distannanes. Here, we report a new nickel-catalysed stannylation of aryl and alkenyl-halides using Bu3SnOMe as a stannyl source to afford aryl and vinyl-stannanes, respectively. This method enables the stannylation of not only bromides, but also chlorides and triflates to furnish functionalized aryl- and alkenyl-stannanes without the release of wasteful and toxic stannyl byproducts.

TYK2 INHIBITORS AND USES THEREOF

-

Paragraph 001223; 001224, (2015/09/28)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

Convenient syntheses of aryl and perfluoroaryl trichlorogermanes and germatranes via an organotin route

Kultyshev, Roman G.,Prakash, G.K. Surya,Olah, George A.,Faller, Jack W.,Parr, Jonathan

, p. 3184 - 3188 (2008/10/09)

Aryl- and (perfluoroaryl)trichlorogermanes ArGeCl3(Ar = C 6H5, 2-FC6H4, 3,5-(CF 3)2C6H3, C6F5, 2,3,5,6-F4C5N) are easily obtained in 60-80% yields from the corresponding tributyl-stannanes and GeCl4 (1:1) at 150 °C in the absence of a solvent. Although the tin-to-germanium transmetalation of C6F5 group is sluggish, it is facilitated by addition of 1-2 mol % AIBN (2,2′-azobis(isobutyronitrile)).

Thiostannylation of arynes with stannyl sulfides: Synthesis and reaction of 2-(arylthio)arylstannanes

Yoshida, Hiroto,Terayama, Tsuguaki,Ohshita, Joji,Kunai, Atsutaka

, p. 1980 - 1981 (2008/10/09)

Arynes were found to insert into a sulfur-tin σ-bond of stannyl sulfides to give a variety of 2-(arylthio)arylstannanes, whose carbon-tin bonds were applicable to further transformations.

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