74233-41-3 Usage
Uses
Used in Chemical Industry:
3,5,5-Trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one is used as a solvent for various applications, including the production of adhesives, paints, and pesticides. Its solubility and reactivity make it a versatile compound in the chemical industry.
Used in Adhesives:
3,5,5-Trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one is used as a solvent in the formulation of adhesives to improve their performance and bonding capabilities. Its ability to dissolve various components and its compatibility with different materials make it an essential ingredient in adhesive formulations.
Used in Paints and Coatings:
3,5,5-Trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one is used as a solvent in paint and coating formulations to enhance their drying time, flow, and leveling properties. Its low toxicity and high solvency make it a preferred choice for paint manufacturers.
Used in Pesticides:
3,5,5-Trimethyl-4-(3-oxobutyl)cyclohex-2-en-1-one is used as a solvent in the formulation of pesticides to improve their effectiveness and stability. Its ability to dissolve active ingredients and its compatibility with various pesticide formulations make it a valuable component in the agrochemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 74233-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,3 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 74233-41:
(7*7)+(6*4)+(5*2)+(4*3)+(3*3)+(2*4)+(1*1)=113
113 % 10 = 3
So 74233-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O2/c1-9-7-11(15)8-13(3,4)12(9)6-5-10(2)14/h7,12H,5-6,8H2,1-4H3
74233-41-3Relevant academic research and scientific papers
Reactions of endocyclic linearly conjugated dienolates with Michael acceptors leading to bicyclo[2.2.2] octane derivatives. Application to the synthesis of C13 degradation products of carotenoids
Ito, Nobuhiko,Etoh, Takeaki
, p. 2397 - 2405 (2007/10/03)
The endocyclic linearly conjugated dienolates from substituted cyclohex-2-enones react with but-3-en-2-one, substituted methyl propenoates, but-3-yn-2-one and methyl propiolate to afford bicyclo[2.2.2]-oct-2-en-1-ols 10a-c, 14a-c and bicyclo[2.2.2]octa-2,5-dien-1-ols 15a,b. The AlCl3-catalysed reaction of 3,5,5-trimethyl-Htrimethylsiloxy)cyclohexa-l)3-diene 3 with (E)-4-acetoxy- and (E)-4-methoxy-but-3-en-2-one provides trans-8-acetoxy-7-acetyl-3,5,5-trimethyl-1-(trimethylsiloxy)bicyclo[2.2.2]oct-2- enes 22, 23 and trans-7-acetyl-8-methoxy-3,5,5-trimethyl-1-(trimethylsiloxy)bicyclo[2.2.2]oct-2- enes 24, 25. Starting from these bicyclo[2.2.2]octenes, the C13 degradation products of carotenoids including 3-oxo-α-ionone 20, blumenol-C 27 and 1,3,7,7-tetramethyl-2-oxabicyclo[4.4.0]decan-9-one 29 have been synthesized.
