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Quinoline, 2-butyl-4-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30980-47-3

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30980-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30980-47-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,9,8 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30980-47:
(7*3)+(6*0)+(5*9)+(4*8)+(3*0)+(2*4)+(1*7)=113
113 % 10 = 3
So 30980-47-3 is a valid CAS Registry Number.

30980-47-3SDS

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 2-butyl-4-methylquinoline

1.2 Other means of identification

Product number -
Other names 2-Butyl-4-methylchinolin

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:30980-47-3 SDS

30980-47-3Downstream Products

30980-47-3Relevant academic research and scientific papers

Tetrakis(trimethylsilyl)silane-Mediated Photochemical Alkylation of Heteroaromatic Bases with Alkyl Halides

Togo, Hideo,Hayashi, Ken,Yokoyama, Masataka

, p. 2063 - 2064 (1991)

Alkyl halides reacted with protonated heteroaromatic bases in the presence of tetrakis(trimethylsilyl)silane (TTMS) under irradiation with high pressure mercury lamp to give the corresponding alkylated heteroaromatic bases.This is the first report on the

The Alkylation and Reduction of Heteroarenes with Alcohols Using Photoredox Catalyzed Hydrogen Atom Transfer via Chlorine Atom Generation

Zidan, Montserrat,Morris, Avery O.,McCallum, Terry,Barriault, Louis

supporting information, p. 1453 - 1458 (2019/08/01)

Radical additions to heteroaromatic bases are frequently employed for the rapid synthesis of complex products using C–H functionalization strategies. The conditions that are commonly employed are typically harsh, routinely requiring stoichiometric oxidants and other additives. In search for milder reaction environments allowing late-stage functionalization, we present the alkylation of N-heteroarenes using primary alcohols and ethers as radical precursors, where the corresponding alkyl radical is formed via hydrogen atom transfer process with a photoredox catalyzed chlorine atom generation as HAT agent. Furthermore, we explore the reduction of the heteroarenes in moderate to high yields when using secondary alcohols.

Recyclable catalytic synthesis of substituted quinolines: copper-catalyzed heterocyclization of 1-(2-aminoaryl)-2-yn-1-ols in ionic liquids

Gabriele, Bartolo,Mancuso, Raffaella,Lupinacci, Elvira,Spina, Rosella,Salerno, Giuseppe,Veltri, Lucia,Dibenedetto, Angela

experimental part, p. 8507 - 8512 (2010/01/06)

A convenient and simple approach for the recyclable catalytic synthesis of substituted quinolines is presented. The method is based on CuCl2-catalyzed heterocyclization of readily available 1-(2-aminoaryl)-2-yn-1-ols in BmimBF4 as the solvent at 100 °C for 15-24 h. The solvent-catalyst system could be successfully recycled up to six times without significant loss of activity.

A NEW GENERAL METHOD OF HOMOLYTIC ALKYLATION OF PROTONATED HETEROAROMATIC BASES

Castaldi, Graziano,Minisci, Francesko,Tortelli, Vito,Vismara, Elena

, p. 3897 - 3900 (2007/10/02)

Alkyl iodides and benzoyl peroxides provide a new general method of homolytic alkylation of protonated heteroaromatic bases.Yields are good and the substitution is selective in the positions ortho and para to the heteroatom.

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