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Quinoline, 1-acetyl-1,2,3,4-tetrahydro-4-methyl- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

135579-07-6

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135579-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135579-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,5,7 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135579-07:
(8*1)+(7*3)+(6*5)+(5*5)+(4*7)+(3*9)+(2*0)+(1*7)=146
146 % 10 = 6
So 135579-07-6 is a valid CAS Registry Number.

135579-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-methyl-3,4-dihydro-2H-quinolin-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-Methyl-3,4-dihydroquinolin-1(2H)-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:135579-07-6 SDS

135579-07-6Downstream Products

135579-07-6Relevant academic research and scientific papers

Visible Light Photocatalytic Synthesis of Tetrahydroquinolines Under Batch and Flow Conditions

González-Mu?oz, Daniel,Nova-Fernández, José Luis,Martinelli, Ada,Pascual-Coca, Gustavo,Cabrera, Silvia,Alemán, José

, p. 5995 - 5999 (2020/09/17)

In this work, we describe the use of visible light and a photocatalytic system for the cyclization of iodoaryl vinyl derivatives to tetrahydroquinoline structures. The reaction proceeds under very mild conditions, tolerates different functional groups and more importantly, the method allows the synthesis of N-free tetrahydroquinolines from N-unprotected starting materials. In addition, the reaction can also be performed using flow-chemistry. Finally, a mechanistic proposal based on some mechanistic studies has been described.

Aryl radical cyclisations: Quinoline, isoquinolone, and 1-benzazepin-2-one rings via 6- and 7-exo cyclisations

Clark,Jones,McCarthy,Storey

, p. 2829 - 2832 (2007/10/02)

The cyclisation of aryl radicals derived by treatment of aryl halides (1a), (1b), (4), (7a), (7b), and (10) with tri-n-butyltin hydride has been investigated.

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