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

65845-73-0

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65845-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65845-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,8,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 65845-73:
(7*6)+(6*5)+(5*8)+(4*4)+(3*5)+(2*7)+(1*3)=160
160 % 10 = 0
So 65845-73-0 is a valid CAS Registry Number.

65845-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4-(2-phenylethyl)quinoline

1.2 Other means of identification

Product number -
Other names 2-Methyl-4-phenethylchinolin

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:65845-73-0 SDS

65845-73-0Downstream Products

65845-73-0Relevant academic research and scientific papers

A Metal-Free Approach for Bronsted Acid Promoted C-H Alkylation of Heteroarenes with Alkyl Peroxides

Zeng, Yuehua,Qian, Bo,Li, Yajun,Bao, Hongli

, p. 3250 - 3256 (2018/06/08)

A metal-free protocol for Minisci C-H alkylation of heteroarenes using alkyl peroxides as the alkylating reagents and internal oxidants simultaneously under promotion of Bronsted acid has been demonstrated. A series of alkyl substituted heteroarenes were readily prepared by the C-H alkylation in moderate to good yields. A possible pathway involving the addition of alkyl radical to heterocycle followed by rearomatization is described.

Synthesis of Functionalized Quinolines through a Reaction of Amides and Alkynes Promoted by Triflic Anhydride/Pyridine

Li, Lian-Hua,Niu, Zhi-Jie,Liang, Yong-Min

supporting information, p. 15300 - 15304 (2017/10/20)

A concise, novel and flexible metal-free single step to synthesize functionalized quinolines is reported. Triflic anhydride-mediated (Tf2O) activation of amides is discussed in the presence of pyridine to offer strong electrophiles, thereby showcasing excellent productivity, high regio- and chemoselectivity, and widely tolerable substrates. This approach provides a straightforward and efficient way to construct azaheterocycle structures.

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