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(6Z)-6-[(butylamino)methylidene]cyclohexa-2,4-dien-1-one - copper (2:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13986-33-9

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13986-33-9 Usage

Uses

Used in Coordination Chemistry:
Used in Catalysis:
Used in Pharmaceutical Applications:
Used in Material Science:
Used in Analytical Chemistry:
(6Z)-6-[(butylamino)methylidene]cyclohexa-2,4-dien-1-one copper (2:1) may also find applications in analytical chemistry as a reagent or reference compound. Its distinct chemical and physical properties can be utilized for the development of new analytical methods, such as spectroscopic or chromatographic techniques, for the detection and quantification of various substances.

Check Digit Verification of cas no

The CAS Registry Mumber 13986-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,8 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13986-33:
(7*1)+(6*3)+(5*9)+(4*8)+(3*6)+(2*3)+(1*3)=129
129 % 10 = 9
So 13986-33-9 is a valid CAS Registry Number.

13986-33-9SDS

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 (6Z)-6-(butylaminomethylidene)cyclohexa-2,4-dien-1-one,copper

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13986-33-9 SDS

13986-33-9Downstream Products

13986-33-9Relevant academic research and scientific papers

Tribochemically active chelate complexes of salicylideneimines

Garnovskii,Burlov,Lysenko,Garnovskii,Borodkina,Ponomarenko,Chigarenko,Nikolaevskii,Minkin

, p. 120 - 127 (2009/07/10)

N-Alkylsalicylideneimines and their complexes with 3d metals were obtained by chemical (from metal salts) and electrochemical methods (from metals in the zero oxidation state). The compounds obtained were characterized by IR and 1H NMR spectros

Mechanism of Formation of Schiff Base Complexes. Part 3. Kinetic Template Effect of Copper(II) in the Condensation Reaction of the Salicylaldehydato-ion with a Polyfunctional Diprimary Amine

Rotondo, Enrico,Priolo, Francesca Cusmano

, p. 1825 - 1828 (2007/10/02)

Under suitable experimental conditions the reaction of the salicylaldehydato-ion (sal) with diethylenetriamine (dien) in the presence of copper(II) takes place trough a first-order kinetic process.The reactants are envisaged as being first co-ordinated to the copper(II), forming a labile ternary complex; interligand condensation is then supposed to occur within the co-ordination sphere of the metal.In the resulting reaction sequence the metal ion functions as a rudimentary enzyme.The dramatic difference between the activity if an ideal enzyme system, which reduces the order of a reaction by one unit through the rapid formation of ternarycomplex, and that of the copper(II) ion, which through an analogous mechanism promotes the reaction of sal and dien, is interpreted on the basis of a perturbation from the optimum reaction geometry of the reactants by the co-ordination of the functional groups to the metal.

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