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116632-52-1

1-(2-methylquinolin-6-yl)ethanone, also known as 2-Me-6-MQA, is an organic compound characterized by the chemical formula C13H11NO. This yellow solid exhibits a distinct odor and is recognized for its significance in the fields of pharmaceuticals, agrochemicals, and organic chemistry. Its molecular structure, which includes a quinoline ring and a ketone group, renders it a valuable intermediate for the synthesis of complex molecules and a subject of interest in drug discovery and synthesis.

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  • 116632-52-1 Structure

  • Basic information

    1. Product Name: 1-(2-methylquinolin-6-yl)ethanone
    2. Synonyms: 1-(2-methylquinolin-6-yl)ethanone
    3. CAS NO:116632-52-1
    4. Molecular Formula:
    5. Molecular Weight: 185.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116632-52-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(2-methylquinolin-6-yl)ethanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-methylquinolin-6-yl)ethanone(116632-52-1)
    11. EPA Substance Registry System: 1-(2-methylquinolin-6-yl)ethanone(116632-52-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 116632-52-1(Hazardous Substances Data)

116632-52-1 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-(2-methylquinolin-6-yl)ethanone is utilized as a building block for the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of novel drugs and chemical products. Its unique structural properties facilitate the creation of diverse compounds with potential therapeutic and pesticidal applications.
Used in Organic Chemistry:
In the realm of organic chemistry, 1-(2-methylquinolin-6-yl)ethanone serves as a versatile intermediate for the synthesis of complex molecules. Its quinoline ring and ketone group provide a foundation for further chemical modifications and the exploration of new synthetic pathways.
Used in Drug Discovery and Synthesis:
1-(2-methylquinolin-6-yl)ethanone's structure and properties make it an important molecule in the study of drug discovery and synthesis. Its potential applications in this field include the development of new therapeutic agents and the enhancement of existing drug formulations.
Used in Material Science and Chemical Processes:
Due to its unique structural properties, 1-(2-methylquinolin-6-yl)ethanone may also have potential applications in the development of new materials and chemical processes. Its integration into these fields could lead to advancements in material science and the optimization of chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 116632-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,6,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 116632-52:
(8*1)+(7*1)+(6*6)+(5*6)+(4*3)+(3*2)+(2*5)+(1*2)=111
111 % 10 = 1
So 116632-52-1 is a valid CAS Registry Number.

116632-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylquinolin-6-yl) ethanone

1.2 Other means of identification

Product number -
Other names 1-(2-methyl-quinolin-6-yl)-ethanone

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:116632-52-1 SDS

116632-52-1Downstream Products

116632-52-1Relevant articles and documents

Hydrogenation of quinolines using a recyclable phosphine-free chiral cationic ruthenium catalyst: Enhancement of catalyst stability and selectivity in an ionic liquid

Zhou, Haifeng,Li, Zhiwei,Wang, Zhijian,Wang, Tianli,Xu, Lijin,He, Yanmei,Fan, Qing-Hua,Pan, Jie,Gu, Lianquan,Chan, Albert S. C.

, p. 8464 - 8467 (2008)

(Chemical Equation Presented) Liquid assets: The catalyst (S,S)-1 exhibits an unprecedented reactivity and excellent enantioselectivity for the title reaction when it is carried out in neat ionic liquid (see scheme; BMIM=1-n-butyl-3-methylimidazolium, Tf=trifluoromethanesulfonyl, Ts=4-toluenesulfonyl). The ionic liquid facilitates the catalyst recycling and enhances its stability and selectivity.

Traceless Directing-Group Strategy in the Ru-Catalyzed, Formal [3 + 3] Annulation of Anilines with Allyl Alcohols: A One-Pot, Domino Approach for the Synthesis of Quinolines

Kumar, Gangam Srikanth,Kumar, Pravin,Kapur, Manmohan

supporting information, p. 2494 - 2497 (2017/05/24)

A unique, ruthenium-catalyzed, [3 + 3] annulation of anilines with allyl alcohols in the synthesis of substituted quinolines is reported. The method employs a traceless directing group strategy in the proximal C-H bond activation and represents a one-pot Domino synthesis of quinolines from anilines.

Assembly of Diversely Substituted Quinolines via Aerobic Oxidative Aromatization from Simple Alcohols and Anilines

Li, Jixing,Zhang, Jinlong,Yang, Huameng,Jiang, Gaoxi

supporting information, p. 3284 - 3290 (2017/03/23)

An aerobic oxidative aromatization of simple aliphatic alcohols and anilines under the Pd(OAc)2/2,4,6-Collidine/Br?nsted acid catalytic system has been established, providing a direct approach for the preparation of diverse substituted quinoline derivatives in high yields with wide functional group tolerance. Practically, the protocol can be easily scaled up to gram-scale and was utilized in the concise formal synthesis of a promising herbicide candidate.

Assembly of substituted 2-alkylquinolines by a sequential palladium-catalyzed Ci-N and Ci-C bond formation

Matsubara, Yoshio,Hirakawa, Saori,Yamaguchi, Yoshihiro,Yoshida, Zen-Ichi

experimental part, p. 7670 - 7673 (2011/10/05)

Diversity: A range of substituted 2-alkylquinolines can be prepared in a general and efficient synthetic approach that employs mild reaction conditions (see scheme). The synthesis is based on a sequential palladium-catalyzed Ci-N and Ci-C bond formation, followed by palladium-catalyzed aromatization, and results in the formation of the desired compounds in one step. Copyright

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