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1983-10-4

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1983-10-4 Usage

Uses

Tri-n-butyltin fluoride is a reagent used for the selective desilylation of bis(silyl) enol ethers. It is also used as antifoulant for marine paints; reagent.

General Description

A liquid.

Reactivity Profile

Fluorotributyltin is in the family of tin compounds widely used as stabilizers for plastics, additives to paint(as antifouling agents). Some have catalytic properties. Examples include butyl tin, dibutyl tin oxide. Their main hazard is associated with their high toxicity, in skin adsorption or inhalation. Fluorotributyltin is incompatible with strong oxidizers like: ammonium nitrate, barium nitrate, barium chlorate, etc.

Safety Profile

Poison by ingestion. Many tributyl tin compounds are hghly toxic to marine life. Mutation data reported.When heated to decomposition it emits toxic fumes of F-. See also TIN COMPOUNDS and FLUORIDES.

Check Digit Verification of cas no

The CAS Registry Mumber 1983-10-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,8 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1983-10:
(6*1)+(5*9)+(4*8)+(3*3)+(2*1)+(1*0)=94
94 % 10 = 4
So 1983-10-4 is a valid CAS Registry Number.
InChI:InChI=1/3C4H9.FH.Sn/c3*1-3-4-2;;/h3*1,3-4H2,2H3;1H;/q;;;;+1/p-1/rC12H27FSn/c1-4-7-10-14(13,11-8-5-2)12-9-6-3/h4-12H2,1-3H3

1983-10-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (T0678)  Tributyltin Fluoride  >95.0%(W)

  • 1983-10-4

  • 25g

  • 920.00CNY

  • Detail
  • Alfa Aesar

  • (39602)  Tri-n-butyltin fluoride   

  • 1983-10-4

  • 5g

  • 222.0CNY

  • Detail
  • Alfa Aesar

  • (39602)  Tri-n-butyltin fluoride   

  • 1983-10-4

  • 25g

  • 936.0CNY

  • Detail
  • Alfa Aesar

  • (39602)  Tri-n-butyltin fluoride   

  • 1983-10-4

  • 100g

  • 2181.0CNY

  • Detail

1983-10-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Fluorotributyltin

1.2 Other means of identification

Product number -
Other names FLUOROTRI-N-BUTYLTIN

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:1983-10-4 SDS

1983-10-4Relevant articles and documents

NEW ANHYDROUS FLUORINATING SYSTEMS: THE COMBINATION OF CROWN-ETHERS AND CESIUM FLUORIDE. A RELATIVE RATE STUDY.

Gingras, Marc,Harpp, David N.

, p. 4669 - 4672 (1988)

New, anhydrous fluorinating systems are presented. 18-Crown-6 or dibenzo-24-crown-8 act as solid - liquid phase transfer catalysts with cesium fluoride.A catalytic amount of these crown ethers with CsF increased the rate of fluorodestannylation of trialkyltin mercaptides (used as a good fluoride probe) by a factor of 5-7.In addition, alkyl bromides, such as benzyl bromide, reacted in a similar way.Kinetic evidence for "sandwich" or "edge" complexes with the cesium cation and 18-crown-6 is presented.

Dunn,Oldfield

, p. 459 (1970)

Fluoro-Substituted Methyllithium Chemistry: External Quenching Method Using Flow Microreactors

Colella, Marco,Degennaro, Leonardo,Higuma, Ryosuke,Ishikawa, Susumu,Luisi, Renzo,Nagaki, Aiichiro,Takahashi, Yusuke,Tota, Arianna

supporting information, p. 10924 - 10928 (2020/05/08)

The external quenching method based on flow microreactors allows the generation and use of short-lived fluoro-substituted methyllithium reagents, such as fluoromethyllithium, fluoroiodomethyllithium, and fluoroiodostannylmethyllithium. Highly chemoselective reactions have been developed, opening new opportunities in the synthesis of fluorinated molecules using fluorinated organometallics.

Palladium complex-catalyzed germylation of allylic halides using (germyl)stannanes

Nakano, Taichi,Ono, Kazuyoshi,Senda, Yoshiya,Migita, Toshihiko

, p. 313 - 317 (2007/10/03)

(Triethylgermyl)tributylstannane reacts metal-selectively with allylic halides at room temperature (r.t.) in the presence of tris(dibenzylideneacetone)dipalladium, Pd2(dba)3CHCl3, to provide an alternative route to allylge

Antifungal sordaridin derivatives

-

, (2008/06/13)

A compound of formula STR1 wherein Z is a tetrahydro-pyrano group selected from STR2 having antifungal activity processes for their preparation and their use in medicines.

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