Tributyl Vinyl Tin

Tributyl Vinyl Tin Sigma Aldrich

Tributyl Vinyl Tin Sigma Aldrich

Tributyl Vinyl Tin 97 Acros Organics Fisher Scientific

Tributyl Vinyl Tin 97 Acros Organics Fisher Scientific

Tributyl Vinyl Tin C14h30sn Pubchem

Tributyl Vinyl Tin C14h30sn Pubchem

Tributyl 1 Ethoxyvinyl Tin 97674 02 7

Tributyl 1 Ethoxyvinyl Tin 97674 02 7

Tributyl Vinyl Tin 7486 35 3

Tributyl Vinyl Tin 7486 35 3

Tributyl Perfluoroethyl Stannane 97 Sigma Aldrich

Tributyl Perfluoroethyl Stannane 97 Sigma Aldrich

Tributyl Perfluoroethyl Stannane 97 Sigma Aldrich

Tributyl 1 ethoxyvinyl tin is generally immediately available in most volumes.

Tributyl vinyl tin.

Tributyl vinyl tinis one of numerous organo metallic compounds sold by american elements under the trade name ae organo metallics for uses requiring non aqueous solubility such as recent solar energy and water treatment applications. Molecular weight 361 15. As a source of vinyltin reagents early work used vinyl trimethyltin but trimethyltin compounds are avoided nowadays owing to their toxicity. It is a white air stable solid.

271438 aldrich dbid 95085. High purity submicron and nanopowder forms may be considered. Shop a large selection of products and learn more about tributyl vinyl tin 97 acros organics. Optical grade usp and ep bp european pharmacopoeia british.

They have three butyl groups covalently bonded to a tin iv centre. Tributyl vinyl tin is used as a reagent in the palladium catalyzed synthesis of allyl and benzyl ethers. American elements produces to many standard grades when applicable including mil spec military grade. Tributyl vinyl tin c14h30sn cid 81998 structure chemical names physical and chemical properties classification patents literature biological activities.

Pubchem substance id 24856437. Molecular weight 317 10. Acs reagent and technical grade. Linear formula ch 2 chsn ch 3 ch 2 3 3.

Tributyl vinyl stannane tributylstannylethylene vinyltributylstannane cas number 7486 35 3. A general formula for these compounds is n c 4 h 9 3 sn x. Tributyl 1 ethoxyvinyl tin 97 cas number 97674 02 7. Vinyl tributyltin is an organotin compound with the formula bu 3 snch ch 2 bu butyl.

Pubchem substance id 24856628. Beilstein reaxys number 3537662. Tributyl vinyl tin is also a vinyl nucleophile for bromoacetylene and bromoaromatics. Validated by experts validated by users non validated removed by users.

It is used as a source of vinyl anion equivalent in stille coupling reactions. Food agricultural and pharmaceutical grade.

Tributyl 4 5 Dihydrofuran 2 Yl Stannane 97 Sigma Aldrich

Tributyl 4 5 Dihydrofuran 2 Yl Stannane 97 Sigma Aldrich

7486 35 3 Tributyl Vinyl Tin Ethenyl Tributyltin Tributylstannyl Ethene Tributylstannyl Ethylene Ethenyltributylstannane Tributylethenylstannane Tributylvinylstannane Tributylvinyltin Vinyltributylstannane Vinyltributyltin C H Sn Trc

7486 35 3 Tributyl Vinyl Tin Ethenyl Tributyltin Tributylstannyl Ethene Tributylstannyl Ethylene Ethenyltributylstannane Tributylethenylstannane Tributylvinylstannane Tributylvinyltin Vinyltributylstannane Vinyltributyltin C H Sn Trc

Tributyl 1 Ethoxyvinyl Tin 97 Sigma Aldrich

Tributyl 1 Ethoxyvinyl Tin 97 Sigma Aldrich

Cis Tributyl 2 Ethoxyethenyl Stannane 97 Sigma Aldrich

Cis Tributyl 2 Ethoxyethenyl Stannane 97 Sigma Aldrich

Allyltriphenylstannane 97 Sigma Aldrich

Allyltriphenylstannane 97 Sigma Aldrich

Trimethyl Tributylstannyl Silane 97 Sigma Aldrich

Trimethyl Tributylstannyl Silane 97 Sigma Aldrich

Tributyl Methoxymethoxy Methyl Stannane Aldrichcpr Sigma Aldrich

Tributyl Methoxymethoxy Methyl Stannane Aldrichcpr Sigma Aldrich

Vinyl Tributyltin Wikipedia

Vinyl Tributyltin Wikipedia

Tributyl Z 2 Ethoxyvinyl Stannane C16h34osn Chemspider

Tributyl Z 2 Ethoxyvinyl Stannane C16h34osn Chemspider

Reaction Scheme For Synthesis Of Compound 1 Reagents And Conditions Download Scientific Diagram

Reaction Scheme For Synthesis Of Compound 1 Reagents And Conditions Download Scientific Diagram

Tributyltin Hydride Contains 0 05 Bht As Stabilizer 97 Sigma Aldrich

Tributyltin Hydride Contains 0 05 Bht As Stabilizer 97 Sigma Aldrich

Stille Reaction Wikipedia

Stille Reaction Wikipedia

Tributylphenylstannane 97 Tributylphenyltin Sigma Aldrich

Tributylphenylstannane 97 Tributylphenyltin Sigma Aldrich

Trans 1 2 Bis Tributylstannyl Ethene 97 Sigma Aldrich

Trans 1 2 Bis Tributylstannyl Ethene 97 Sigma Aldrich

Tert Butyl 4 Vinylphenyl Carbonate 98 Sigma Aldrich

Tert Butyl 4 Vinylphenyl Carbonate 98 Sigma Aldrich

Synthesis Of Spongistatin 2 Employing A New Route To The Ef Fragment Chemical Science Rsc Publishing Doi 10 1039 C3sc50304f

Synthesis Of Spongistatin 2 Employing A New Route To The Ef Fragment Chemical Science Rsc Publishing Doi 10 1039 C3sc50304f

Application Of Copper I Salt And Fluoride Promoted Stille Coupling Reactions In The Synthesis Of Bioactive Molecules Organic Biomolecular Chemistry Rsc Publishing Doi 10 1039 C9ob01602c

Application Of Copper I Salt And Fluoride Promoted Stille Coupling Reactions In The Synthesis Of Bioactive Molecules Organic Biomolecular Chemistry Rsc Publishing Doi 10 1039 C9ob01602c

Tributyl Trimethylsilylethynyl Tin 81353 38 0 Tci America

Tributyl Trimethylsilylethynyl Tin 81353 38 0 Tci America

Stereocontrolled Synthesis Of Quaternary B G Unsaturated Amino Acids Chain Extension Of D L A 2 Tributylstannyl Vinyl Amino Acids Abstract Europe Pmc

Stereocontrolled Synthesis Of Quaternary B G Unsaturated Amino Acids Chain Extension Of D L A 2 Tributylstannyl Vinyl Amino Acids Abstract Europe Pmc

Oxovanadium Iv Containing Poly Styrene Co 4 Ethenyl 2 Hydroxyphenylimidazole Electrospun Nanofibers For The Catalytic Oxidation Of Thioanisole Sciencedirect

Oxovanadium Iv Containing Poly Styrene Co 4 Ethenyl 2 Hydroxyphenylimidazole Electrospun Nanofibers For The Catalytic Oxidation Of Thioanisole Sciencedirect

Enol Triflates Derived From The Wieland Miescher Ketone And An Analog Bearing An Angular Acetoxymethyl Group Their Highly Regioselective Synthesis And Stille Coupling With Vinyl Tributyl Tin Sciencedirect

Enol Triflates Derived From The Wieland Miescher Ketone And An Analog Bearing An Angular Acetoxymethyl Group Their Highly Regioselective Synthesis And Stille Coupling With Vinyl Tributyl Tin Sciencedirect

Tributyltin Hydride 688 73 3

Tributyltin Hydride 688 73 3

Asymmetric Fluorination Of Indanone 2 Carboxylates Using A Polystyrene Supported Diphenylamine Linked Bis Oxazoline Complex Organic Biomolecular Chemistry Rsc Publishing Doi 10 1039 C8ob01943f

Asymmetric Fluorination Of Indanone 2 Carboxylates Using A Polystyrene Supported Diphenylamine Linked Bis Oxazoline Complex Organic Biomolecular Chemistry Rsc Publishing Doi 10 1039 C8ob01943f

Functionalization Of Imidazo 1 2 A Pyridines By Means Of Metal Catalyzed Cross Coupling Reactions Koubachi 2014 European Journal Of Organic Chemistry Wiley Online Library

Functionalization Of Imidazo 1 2 A Pyridines By Means Of Metal Catalyzed Cross Coupling Reactions Koubachi 2014 European Journal Of Organic Chemistry Wiley Online Library

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