10341-59-0 Usage
Uses
Used in Paints and Coatings Industry:
(Z)-2-Butanone oxime is used as a stabilizer and inhibitor for [application reason] to prevent the premature curing or polymerization of paints and coatings, ensuring a consistent and high-quality finish.
Used in Adhesives Industry:
(Z)-2-Butanone oxime is used as a stabilizer and inhibitor for [application reason] to enhance the shelf life and performance of adhesives, preventing unwanted reactions that could compromise their bonding capabilities.
Used in Polymers Industry:
(Z)-2-Butanone oxime is used as a stabilizer and inhibitor for [application reason] to improve the stability and durability of polymers, reducing the risk of degradation or failure over time.
Used in Alkyd Paints:
(Z)-2-Butanone oxime is used as an anti-skinning agent for [application reason] to prevent the formation of a skin on the surface of the paint in the container, maintaining the paint's consistency and workability.
Used as a Chemical Intermediate:
(Z)-2-Butanone oxime is used as a chemical intermediate for [application reason] in the synthesis of other compounds, contributing to the development of a variety of chemical products.
Used in Metalworking Fluids:
(Z)-2-Butanone oxime has been studied for its potential as a corrosion inhibitor for [application reason] in metalworking fluids, aiming to protect metal surfaces from corrosion and extend the life of machinery and tools.
It is important to handle (Z)-2-Butanone oxime with care, as it can cause skin and eye irritation and may be harmful if ingested or inhaled.
Check Digit Verification of cas no
The CAS Registry Mumber 10341-59-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10341-59:
(7*1)+(6*0)+(5*3)+(4*4)+(3*1)+(2*5)+(1*9)=60
60 % 10 = 0
So 10341-59-0 is a valid CAS Registry Number.
10341-59-0Relevant articles and documents
Synthesis of highly substituted pyrroles via nucleophilic catalysis
Ngwerume, Simbarashe,Camp, Jason E.
supporting information; experimental part, p. 6271 - 6274 (2010/11/19)
Figure presented. A nucleophilic catalysis method providing a concise synthesis of di-, tri-, and tetrasubstituted pyrroles is described. This regioselective one-pot method relies on nucleophilic catalysis of the intermolecular addition of oximes to activ
