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Stannane, bromobutyldimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56931-02-3

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56931-02-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56931-02-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,3 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56931-02:
(7*5)+(6*6)+(5*9)+(4*3)+(3*1)+(2*0)+(1*2)=133
133 % 10 = 3
So 56931-02-3 is a valid CAS Registry Number.

56931-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-bromobutyl(dimethyl)stannane

1.2 Other means of identification

Product number -
Other names Stannane,bromobutyldimethyl

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:56931-02-3 SDS

56931-02-3Upstream product

56931-02-3Downstream Products

56931-02-3Relevant academic research and scientific papers

Electron Donor-Acceptor Complexes. 1. Linear Free Energy Correletion of the Charge-Transfer Transition Energy with the Kinetics of Halogenolysis of Alkylmetals

Fukuzumi, S.,Kochl, J.K.

, p. 2246 - 2254 (2007/10/02)

Mulliken charge-transfer theory is used to relate the properties of transient donor-acceptor complexes between alkylmetals and halogens with the kinetics of the accompanying cleavage reaction (halogenolysis).The formulation derives from the charge-transfer transition energy hνCT which is proportional to the second-order rate constant for halogenolysis of a variety of tetraalkyltin compounds in hexane or carbon tetrachloride solutions.The description of the activation process for halogenolysis as an electron transfer in the CT complex, e.g., --> , leads to a linear free energy relationship in which the activation free energy is equal to the driving force for ion pair formation.The latter is equated to the charge-transfer transition energy plus a contribution from the solvation energy, by employing a comparative procedure for the evaluation of alkylmetals.An independent measure of the solvation energy obtained from the gas-phase ionization potentials of alkylmetals and their free energy changes in solution supports the electron-transfer formulation of the activation process.The charge-transfer mechanism is generalized for the halogenolysis of alkylmetals.

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