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88565-88-2

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88565-88-2 Usage

General Description

4,6,8-Trimethylquinoline is a chemical compound with a molecular formula C13H11N. It is a derivative of quinoline, and is known for its orange-yellowish appearance. 4,6,8-Trimethylquinoline is often used as a fragrance ingredient in perfumes and as a flavoring agent in foods. It is also used in the production of dyes, pharmaceuticals, and rubber chemicals. In addition, 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. However, it is important to handle this compound with care as it may be harmful if ingested or inhaled and can cause skin and eye irritation.

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

88565-88-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6,8-Trimethylquinoline

1.2 Other means of identification

Product number -
Other names 4,6,8-Trimethyl-chinolin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88565-88-2 SDS

88565-88-2Relevant articles and documents

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.

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