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Ethanone, 1,1-(2,3-pyridinediyl)bis- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16174-40-6

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16174-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16174-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,7 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16174-40:
(7*1)+(6*6)+(5*1)+(4*7)+(3*4)+(2*4)+(1*0)=96
96 % 10 = 6
So 16174-40-6 is a valid CAS Registry Number.

16174-40-6SDS

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 1,1'-pyridine-2,3-diyl-bis-ethanone

1.2 Other means of identification

Product number -
Other names 1-(3-Acetyl-pyridin-2-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:16174-40-6 SDS

16174-40-6Downstream Products

16174-40-6Relevant academic research and scientific papers

Metal-free C-H methylation and acetylation of heteroarenes with PEG-400

Kudale, Vishal Suresh,Wang, Jeh-Jeng

supporting information, p. 3506 - 3511 (2020/06/25)

The generation of a methyl carbon source from renewable and cheap sources is challenging. Herein, we describe a novel and an efficient route for methylation and acetylation of aza-heteroarenes using PEG-400 under O2and TsOH·H2O for the first time by tuning the reaction conditions using a different set of starting materials. The key features of the current protocol are oxidative C-O and C-C bond scission under metal-free conditions with good functional group tolerance, and a broad substrate scope. The potential applicability of the designed methodology was demonstrated for the synthesis of central nervous system (CNS) depressant and anticonvulsant drug molecules by a one-pot strategy.

Ozonolysis of Quinolines: A Versatile Synthesis of Polyfunctional Pyridines

O'Murchu, C.

, p. 880 - 882 (2007/10/02)

A simple, safe and efficient procedure, easily adapted to a large scale, is described for the synthesis of substituted quinolines 2, which are readily oxidized by ozone in the presence of mineral acid, followed by an oxidative work up with hydrogen peroxide to afford substituted 2,3-pyridinedicarboxylic acids 3a-d,f and acyl pyridines 3e, g.

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