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4-Methyl-quinoline-6-carboxylic acid is an organic compound with the chemical formula C11H9NO2. It is a derivative of quinoline, a heterocyclic aromatic compound consisting of a benzene ring fused to a pyridine ring. The molecule features a methyl group at the 4-position and a carboxylic acid group at the 6-position. 4-Methyl-quinoline-6-carboxylic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. It is also used as an intermediate in the preparation of other quinoline-based compounds. Due to its chemical structure, 4-methyl-quinoline-6-carboxylic acid exhibits unique properties and reactivity, making it a valuable building block in organic synthesis.

7101-68-0

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7101-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7101-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,0 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7101-68:
(6*7)+(5*1)+(4*0)+(3*1)+(2*6)+(1*8)=70
70 % 10 = 0
So 7101-68-0 is a valid CAS Registry Number.

7101-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylquinoline-6-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-methyl-6-quinolinecrboxylic acid

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:7101-68-0 SDS

7101-68-0Relevant academic research and scientific papers

Metal-Free Chemoselective Oxidation of 4-Methylquinolines into Quinoline-4-Carbaldehydes

Xu, Jincheng,Li, Yang,Ding, Tianling,Guo, Hao

, p. 3114 - 3117 (2021/09/03)

A convenient protocol for the synthesis of quinoline-4-carbaldehydes via chemoselective oxidation of 4-methylquinolines using hypervalent iodine(III) reagents as oxidant is described. This method highlights metal-free and mild reaction conditions, nice yield, good functional group tolerance, and high chemoselectivity.

Nanocatalosomes as Plasmonic Bilayer Shells with Interlayer Catalytic Nanospaces for Solar-Light-Induced Reactions

Cho, Yoon-Kyoung,Dubbu, Sateesh,Kim, Inki,Koo, Jung Hun,Kumar, Amit,Kumar, Sumit,Kumari, Nitee,Kwon, Taewan,Lee, In Su,Lim, Jongwon,Rho, Junsuk

supporting information, p. 9460 - 9469 (2020/05/04)

Interest and challenges remain in designing and synthesizing catalysts with nature-like complexity at few-nm scale to harness unprecedented functionalities by using sustainable solar light. We introduce “nanocatalosomes”—a bio-inspired bilayer-vesicular design of nanoreactor with metallic bilayer shell-in-shell structure, having numerous controllable confined cavities within few-nm interlayer space, customizable with different noble metals. The intershell-confined plasmonically coupled hot-nanospaces within the few-nm cavities play a pivotal role in harnessing catalytic effects for various organic transformations, as demonstrated by “acceptorless dehydrogenation”, “Suzuki–Miyaura cross-coupling” and “alkynyl annulation” affording clean conversions and turnover frequencies (TOFs) at least one order of magnitude higher than state-of-the-art Au-nanorod-based plasmonic catalysts. This work paves the way towards next-generation nanoreactors for chemical transformations with solar energy.

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