18217-12-4 Usage
Uses
Used in Coatings Industry:
5-Methyl-2-heptanone is used as a solvent to dissolve and reduce the viscosity of coatings, improving their application properties and drying time.
Used in Adhesives Industry:
In the adhesives industry, 5-Methyl-2-heptanone is used as a solvent to adjust the consistency and bonding strength of adhesive formulations, enhancing their performance on various substrates.
Used in Industrial Cleaning:
5-Methyl-2-heptanone is utilized as a cleaning agent in industrial settings to remove grease, oil, and other contaminants from machinery and equipment, ensuring efficient operation and maintenance.
Used as a Chemical Intermediate:
5-Methyl-2-heptanone serves as a chemical intermediate in the synthesis of various chemicals, including pharmaceuticals and pesticides, contributing to the development of new products and applications.
It is important to handle and store 5-Methyl-2-heptanone with proper safety measures to prevent irritation to the eyes, skin, and respiratory system, as it is considered relatively low in toxicity but can cause such effects upon exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 18217-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,1 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18217-12:
(7*1)+(6*8)+(5*2)+(4*1)+(3*7)+(2*1)+(1*2)=94
94 % 10 = 4
So 18217-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-4-7(2)5-6-8(3)9/h7H,4-6H2,1-3H3
18217-12-4Relevant academic research and scientific papers
Preparation and reactivity of cyanocuprates containing alkylseleno and alkyltelluro groups as non-transferable ligands
Zinn, Fabiano K.,Ramos, Eduardo C.,Comasseto, Jo?o V.
, p. 2415 - 2417 (2007/10/03)
Alkylseleno and alkyltelluro groups are efficient non-transferable ligands of cyanocuprates in 1,4-addition reactions to enones.
Diisopropoxyaluminium trifluoroacetate/4-nitrobenzaldehyde - A new Oppenauer oxidation system for accelerated oxidation of secondary alcohols to the corresponding ketones
Akamanchi, Krishnacharya G.,Chaudhari, Bapu A.
, p. 6925 - 6928 (2007/10/03)
A practical, efficient and accelerated oxidation of secondary alcohols to the corresponding ketones has been achieved at rt in high yields by a modified Oppenauer oxidation system using diisopropoxyaluminium trifluoroacetate as catalyst and 4-nitrobenzaldehyde as a hydride acceptor.
PHOTOSENSITIZED OXIDATION OF 3,6-DIMETHYLOCTANE
Rontani, J-F.,Giusti, G.
, p. 1923 - 1926 (2007/10/02)
In this paper an interesting mechanism involving a Barton reaction wich leads to a propagation of photooxidation processes between γ-positioned tertiary carbons is described.
CONJUGATE ADDITION TO α,β-UNSATURATED KETONES WITH MIXED LITHIUM TRIORGANOZINCATES
Watson, Randall A.,Kjonaas, Richard A.
, p. 1437 - 1440 (2007/10/02)
Lithium Triorganozincates of the type RR'2ZnLi, where R'=Me and R=n-Bu or sec-Bu, efficiently transfer the R group in a 1,4 fashion to α,β-unsaturated ketones.
