62831-62-3 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Cyclohexanedione, 4-(1-methylethyl)is used as an intermediate in the synthesis of pharmaceuticals for its ability to inhibit the activity of certain enzymes, contributing to the development of new drugs.
Used in Agrochemical Industry:
1,3-Cyclohexanedione, 4-(1-methylethyl)is used as an intermediate in the synthesis of agrochemicals, playing a role in the development of pesticides or other agricultural chemicals to improve crop protection and yield.
Used in Organic Compounds Synthesis:
1,3-Cyclohexanedione, 4-(1-methylethyl)is utilized as an intermediate in the synthesis of various organic compounds, contributing to the creation of a wide range of chemical products.
Used in Medicinal Chemistry Research:
Due to its enzyme inhibitory properties, 1,3-Cyclohexanedione, 4-(1-methylethyl)is used in medicinal chemistry research to explore its potential in the development of treatments for various diseases and conditions.
Used for Antioxidant and Antimicrobial Applications:
Leveraging its antioxidant and antimicrobial properties, 1,3-Cyclohexanedione, 4-(1-methylethyl)can be used in the development of products that require these characteristics, such as preservatives, disinfectants, or additives in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 62831-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,3 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62831-62:
(7*6)+(6*2)+(5*8)+(4*3)+(3*1)+(2*6)+(1*2)=123
123 % 10 = 3
So 62831-62-3 is a valid CAS Registry Number.
62831-62-3Relevant academic research and scientific papers
Synthesis of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones
Piers, Edward,Grierson, John R.,Lau, Cheuk Kun,Nagakura, Isao
, p. 210 - 223 (2007/10/02)
A new, efficient method for the preparation of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketones is described.The method involves the reaction of β-diketones or α-hydroxymethylenecycloalkanones with triphenylphosphine dihalides in the presence of trie
