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994-89-8

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994-89-8 Usage

Description

TRIBUTYLSTANNYLACETYLENE, also known as Ethynyltributylstannane, is an organotin compound with the chemical formula Bu3SnC≡CH. It is a clear colorless liquid and is used as a versatile reagent in organic synthesis.

Uses

Used in Organic Synthesis:
TRIBUTYLSTANNYLACETYLENE is used as an ethynylation reagent for azaaromatics, enabling the formation of various organic compounds.
Used in the Preparation of Vinylstannanes and Stannylisoxazoles:
TRIBUTYLSTANNYLACETYLENE is used as a reactant to prepare vinylstannanes and stannylisoxazoles, which are important intermediates in organic synthesis.
Used in the Synthesis of Terminal Arylacetylene Derivatives:
TRIBUTYLSTANNYLACETYLENE is used in the Stille coupling reaction with aryl halides in the presence of a palladium catalyst to produce terminal arylacetylene derivatives.
Used in the Synthesis of 1,4-bis(tributylstannyl)but-1-yne:
TRIBUTYLSTANNYLACETYLENE is used in the dimerization process using a metal complex with bulky ligand catalyst system to form 1,4-bis(tributylstannyl)but-1-yne.
Used in the Synthesis of Isoquinolone Derivatives:
TRIBUTYLSTANNYLACETYLENE is used in the reaction with benzotriazinones via denitrogenative insertion in the presence of a nickel catalyst to produce isoquinolone derivatives.
Used in the Total Synthesis of (-)-Acutumine and (-)-Dechloroacutumine:
TRIBUTYLSTANNYLACETYLENE is used as an enyne key intermediate in the total synthesis of (-)-acutumine and (-)-dechloroacutumine, which are biologically active compounds.

Purification Methods

Purify it by dissolving the reagent (ca 50g) in heptane (250mL), washing it with H2O (100mL), drying (MgSO4), evaporating and distilling in a vacuum. It has IR: max 3280 ( C), 2950, 2850, 2005 (CC), 1455, 1065 and 865cm-1. [Bottaro et al. J Org Chem 46 5221 1981, Stille & Simpson J Am Chem Soc 109 2138 1987, Zavgorodnii et al. J Gen Chem USSR (Engl Edn) 37 1469 1967.]

Check Digit Verification of cas no

The CAS Registry Mumber 994-89-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 994-89:
(5*9)+(4*9)+(3*4)+(2*8)+(1*9)=118
118 % 10 = 8
So 994-89-8 is a valid CAS Registry Number.
InChI:InChI=1/3C4H9.C2H.Sn/c3*1-3-4-2;1-2;/h3*1,3-4H2,2H3;1H;/rC14H28Sn/c1-5-9-12-15(8-4,13-10-6-2)14-11-7-3/h4H,5-7,9-14H2,1-3H3

994-89-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L20178)  Ethynyltri-n-butyltin, 96%   

  • 994-89-8

  • 1g

  • 581.0CNY

  • Detail
  • Alfa Aesar

  • (L20178)  Ethynyltri-n-butyltin, 96%   

  • 994-89-8

  • 5g

  • 1910.0CNY

  • Detail
  • Aldrich

  • (275069)  Ethynyltributylstannane  95%

  • 994-89-8

  • 275069-1G

  • 866.97CNY

  • Detail
  • Aldrich

  • (275069)  Ethynyltributylstannane  95%

  • 994-89-8

  • 275069-5G

  • 2,311.92CNY

  • Detail

994-89-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name TRIBUTYLSTANNYLACETYLENE

1.2 Other means of identification

Product number -
Other names tributyl(ethynyl)stannane

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:994-89-8 SDS

994-89-8Relevant articles and documents

HYDROXAMIC ACID DERIVATIVES AS LPXC INHIBITORS FOR THE TREATMENT OF BACTERIAL INFECTIONS

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Page/Page column 103-104, (2014/10/15)

This invention pertains generally to antibacterial organic compounds of Formula I as described herein, and pharmaceutical compositions containing such compounds. In certain aspects, the invention pertains to treating infections caused by Gram-negative bac

FACTOR IXA INHIBITORS

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Page/Page column 80-81, (2014/08/19)

The present invention provides a compound of Formula (I) (structurally represented) wherein R1 is H or C1-6 alkyl, R2 is H or C1-6 alkyl or CH20H, R3 is H or C1-6 alkyl, and R4 is H or C1-6 alkyl, provided that when R1, R2, and R3 are H, R4 is C1-6 alkyl, and when R1, R2, and R4 are H, then R3 is C1-6 alkyl, and when R1, R3, and R4 are H, R2 is C1-6 alkyl or-CH20H, and when R2, R3, and R4 are H, then R1 is C 1-6 alkyl; A is 1 ) a 9-10 membered bicyclic heterocycle having 1-3 heteroatoms independently selected from N, S and 0, which 9-10 membered bicyclic heterocycle is unsubstituted or substituted with R5 and unsubstituted or substituted with R6 and unsubstituted or substituted with NH2, or 2) a 6-9 membered monocyclic or bicyclic carbocyclic ring system unsubstituted or substituted with R5, unsubstituted or substituted with R6, and unsubstituted or substituted with -CH2NH2; and B is 1) a 5- or 6-membered monocyclic heterocycle having 1 or 2 heteroatoms independently selected from N, S or 0, which is unsubstituted or substituted on a carbon or nitrogen atom with R7, unsubstituted or substituted on a carbon or nitrogen atom with R8, and unsubstituted or substituted on a carbon or nitrogen atom with R9, or 2) an 8- or 9-membered fused bicyclic heterocycle having 1, 2 or 3 nitrogen atoms which is unsubstituted or substituted on a carbon or nitrogen atom with R7, and unsubstituted or substituted on a carbon or nitrogen atom with R8; and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses.

6-substituted mycophenolic acid and derivatives

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, (2008/06/13)

The disclosed 6-substituted derivatives of mycophenolic acid are therapeutic agents advantageous in the treatment of disease states indicated for mycophenolic acid and/or mycophenolate mofetil.

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