88565-88-2 Usage
Uses
Used in Perfumery Industry:
4,6,8-Trimethylquinoline is used as a fragrance ingredient in perfumes for its distinct and appealing scent, enhancing the overall aroma of the product.
Used in Food Industry:
In the food industry, 4,6,8-Trimethylquinoline serves as a flavoring agent, imparting a unique taste to various food products and improving their overall flavor profile.
Used in Dye Production:
4,6,8-Trimethylquinoline is utilized in the production of dyes, contributing to the development of vibrant and long-lasting colorants for various applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 4,6,8-Trimethylquinoline is employed in the synthesis of various drugs, taking advantage of its chemical properties to create effective medicinal compounds.
Used in Rubber Chemicals Production:
4,6,8-Trimethylquinoline is used in the production of rubber chemicals, where it plays a crucial role in enhancing the performance and durability of rubber products.
Used in Medicinal Chemistry Research:
4,6,8-Trimethylquinoline has been studied for its potential antioxidant and neuroprotective properties, making it a subject of interest in the field of medicinal chemistry. Its ability to protect cells from oxidative damage and support brain health has garnered attention for its potential therapeutic applications.
However, it is essential to handle 4,6,8-Trimethylquinoline with care, as it may be harmful if ingested or inhaled and can cause skin and eye irritation. Proper safety measures should be taken during its use to minimize any adverse effects.
Check Digit Verification of cas no
The CAS Registry Mumber 88565-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88565-88:
(7*8)+(6*8)+(5*5)+(4*6)+(3*5)+(2*8)+(1*8)=192
192 % 10 = 2
So 88565-88-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N/c1-8-6-10(3)12-11(7-8)9(2)4-5-13-12/h4-7H,1-3H3
88565-88-2Relevant academic research and scientific papers
Photoredox Neutral Decarboxylative Hydroxyalkylations of Heteroarenes with α-Keto Acids
Ji, Xiaochen,Yang, Zhonglin,Wu, Xinzhuang,Deng, Guo-Jun,Huang, Huawen
supporting information, p. 4168 - 4182 (2022/03/14)
Photoredox neutral decarboxylative hydroxyalkylations of heteroarenes with α-keto acids under mild conditions are described. Stable and readily available α-keto acids were employed as hydroxyalkylating reagents with only CO2released as the byproduct. A range of aromatic and aliphatic α-keto acids were successfully converted into hydroxyalkylated products with various heteroarenes. This transformation proceeded through a decarboxylation/Minisci addition/SCS sequence, generating a variety of valuable hydroxyalkylated heteroarenes.
