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4-[dibutyl(chloro)stannanyl]butan-2-one is a chemical compound with the molecular formula C12H25ClOSn. It is an organotin compound, which is characterized by the presence of a tin atom bonded to organic groups. This specific compound features a butan-2-one (a four-carbon ketone) backbone with a dibutyl(chloro)stannanyl group attached to the fourth carbon. The dibutyl(chloro)stannanyl group consists of a tin atom bonded to two butyl groups and one chlorine atom. Organotin compounds like this are often used as catalysts, stabilizers, or intermediates in organic synthesis. They can also have applications in the production of certain types of polymers and as biocides. Due to their potential environmental and health impacts, the use of organotin compounds is subject to regulation in many countries.

65301-77-1

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65301-77-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65301-77-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,3,0 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65301-77:
(7*6)+(6*5)+(5*3)+(4*0)+(3*1)+(2*7)+(1*7)=111
111 % 10 = 1
So 65301-77-1 is a valid CAS Registry Number.

65301-77-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[dibutyl(chloro)stannyl]butan-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:65301-77-1 SDS

65301-77-1Downstream Products

65301-77-1Relevant academic research and scientific papers

Intramolecular assistance of electron transfer. Oxidative cleavage of the carbon-tin bond of tetraalkylstannanes

Yoshida, Jun-Ichi,Izawa, Mitsuhiko

, p. 9361 - 9365 (1997)

Experimental and theoretical studies of intramolecular assistance by carbonyl groups and heteroatoms in the electron transfer driven cleavage of the carbon-tin bond of tetraalkylstannanes has been carried out. Carbonyl groups and heteroatoms (oxygen and n

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