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6,7-Dimethyl-2-hydroxyquinoline is an organic compound belonging to the class of quinolines, which are heterocyclic compounds with a benzene ring fused to a pyridine ring. 6,7-Dimethyl-2-hydroxyquinoline is characterized by the presence of two methyl groups at the 6th and 7th positions and a hydroxy group at the 2nd position within the quinoline system. It exhibits strong aromatic properties and is typically found in a light yellow to brownish liquid form. Although information on this chemical is limited, it is considered a potentially hazardous substance and should be handled with caution in a controlled environment, adhering to standard safety protocols.

54904-39-1

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54904-39-1 Usage

Uses

Used in Organic Synthesis:
6,7-Dimethyl-2-hydroxyquinoline is used as a key intermediate in the synthesis of various organic compounds. Its unique chemical structure allows it to participate in a range of reactions, making it a valuable building block for the creation of new molecules with potential applications in various industries.
Used in Pharmaceutical Industry:
6,7-Dimethyl-2-hydroxyquinoline is used as a starting material for the development of new pharmaceutical compounds. Its aromatic nature and functional groups make it a promising candidate for the synthesis of drugs with potential therapeutic applications.
Used in Chemical Research:
6,7-Dimethyl-2-hydroxyquinoline is used as a research tool in the field of chemistry. Its properties and reactivity are studied to gain insights into the behavior of similar compounds and to develop new synthetic strategies and methodologies.
Used in Material Science:
6,7-Dimethyl-2-hydroxyquinoline is used as a component in the development of new materials with specific properties. Its incorporation into various systems can lead to the creation of materials with improved characteristics, such as enhanced stability or novel functionalities.
Used in Agrochemical Industry:
6,7-Dimethyl-2-hydroxyquinoline is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its chemical structure can be modified to create compounds with increased efficacy and selectivity, contributing to more effective crop protection strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 54904-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,0 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 54904-39:
(7*5)+(6*4)+(5*9)+(4*0)+(3*4)+(2*3)+(1*9)=131
131 % 10 = 1
So 54904-39-1 is a valid CAS Registry Number.

54904-39-1Relevant academic research and scientific papers

Iron-catalyzed aerobic oxidative cleavage of the C-C σ-bond using air as the oxidant: Chemoselective synthesis of carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds

Xing, Qi,Lv, Hui,Xia, Chungu,Li, Fuwei

, p. 489 - 492 (2016/01/12)

A simple iron-catalyzed aerobic oxidative C-C σ-bond cleavage of ketones has been developed. Readily available and environmentally benign air is used as the oxidant. This reaction avoids the use of noble metal catalysts or specialized oxidants, chemoselectively yielding carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds without overoxidation.

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