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Stannane, trimethyl[(1E)-2-phenylethenyl]-, also known as (1E)-2-phenylethenyltrimethylstannane, is an organotin compound with the chemical formula C11H14Sn. It is a colorless liquid that is sensitive to air and moisture. Stannane, trimethyl[(1E)-2-phenylethenyl]- is primarily used as a reagent in organic synthesis, particularly in the formation of carbon-carbon bonds through the Stille coupling reaction, a widely used method in the synthesis of complex organic molecules. It is also employed as a reducing agent in various chemical reactions. Due to its reactivity, it is essential to handle Stannane, trimethyl[(1E)-2-phenylethenyl]- with care, typically under an inert atmosphere or in a controlled environment.

7422-28-8

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7422-28-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7422-28-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7422-28:
(6*7)+(5*4)+(4*2)+(3*2)+(2*2)+(1*8)=88
88 % 10 = 8
So 7422-28-8 is a valid CAS Registry Number.

7422-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(2-phenylethenyl)stannane

1.2 Other means of identification

Product number -
Other names trimethylstyrylstannane

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:7422-28-8 SDS

7422-28-8Relevant academic research and scientific papers

ORGANOMETALLIC COMPOUNDS. LXXII. REACTIONS OF RACEMIC TETRAORGANOTIN COMPOUNDS WITH BUTYLLITHIUM AND WITH LITHIUM ALUMINUM HYDRIDE

Gielen, Marcel,Tondeur, Yves

, p. 371 - 376 (2007/10/02)

Racemic methylneophylphenyltrityltin (I) reacts with an excess of butyllithium to give dibutylmethylneophyltin (II) in high yield, whereas bifluorenyl-9-ylmethylneophylphenyltin is converted with an excess butyllithium into butylmethylneophylphenyltin (II

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