Welcome to LookChem.com Sign In|Join Free

CAS

  • or

195967-10-3

Post Buying Request

195967-10-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

195967-10-3 Usage

General Description

4-Chloro-2,6-diacetylpyridine is a chemical compound with the molecular formula C7H6ClNO2. It is a chlorinated derivative of 2,6-diacetylpyridine and belongs to the class of pyridine compounds. This chemical is commonly used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various biologically active compounds. It is also used as an intermediate in the production of dyes, pigments, and other specialty chemicals. 4-Chloro-2,6-diacetylpyridine is a yellow solid at room temperature and is considered to be potentially hazardous if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 195967-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,9,6 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 195967-10:
(8*1)+(7*9)+(6*5)+(5*9)+(4*6)+(3*7)+(2*1)+(1*0)=193
193 % 10 = 3
So 195967-10-3 is a valid CAS Registry Number.

195967-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-acetyl-4-chloropyridin-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 2,6-diacetyl-4-chloropyridine

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:195967-10-3 SDS

195967-10-3Downstream Products

195967-10-3Relevant articles and documents

Amphiphilic pentaazamacrocyclic manganese superoxide dismutase mimetics

Lieb, Dominik,Kenkell, Isabell,Miljkovic, Jan Lj.,Moldenhauer, Daniel,Weber, Nadine,Filipovic, Milos R.,Groehn, Franziska,Ivanovic-Burmazovic, Ivana

, p. 1009 - 1020 (2014)

Five newly functionalized pentaazamacrocyclic manganese complexes, with variable lengths and amounts of the aliphatic groups (three compounds with one linear chain containing 12, 16, and 22 carbon atoms, i.e., MnL1, MnL2, and MnL3, respectively, as well as two compounds containing two C12 and C16 chains, MnL4 and MnL5, respectively) that are derivatives of the known SOD mimetic, Mn(Me2-Pyane), have been synthesized. These amphiphilic complexes were characterized by the ESI mass spectrometry, potentiometric titrations, light scattering, cyclic voltammetry, and direct stopped-flow determination of their SOD activity at pH 8.1 and 7.4 (in phosphate and HEPES buffers). The formation of supramolecular aggregates that predominantly exist in the solution as a defined micellar/nanostructure assembly, with an average 400 nm size, has been demonstrated for MnL1. The biological effects of the selected complexes (MnL1 and MnL2) on the superoxide level in cytosol and mitochondria have been tested, as well as their effects on the prevention of the lipid peroxidation induced by paraquat. Advantages and disadvantages of the lipophilic pentaazamacrocyclic manganese SOD mimetics in comparison to the corresponding nonsubstituted SOD active complex have been discussed.

Synthetic Access to Derivatized Mn-Pyane as a Redox-modulated Pool of SODm

Scheitler, Andreas,Friedel, Felix,Puchta, Ralph,Dücker-Benfer, Carlos,Ivanovi?-Burmazovi?, Ivana

, p. 713 - 718 (2018)

In this work, four derivatives of the pentaazamacrocyclic Mn-pyane [pyane = trans-2,13-dimethyl-3,6,9,12,18-pentaazabicyclo[12.3.1]-octadeca-1(18),14,16-triene] complex were synthesized and characterized, carrying small substituents at the pyridine ring that allow fine-tuning of the manganese centered redox potential, without significant change to the overall complex arrangement that is crucial for a correct comparison regarding their superoxide dismutase mimetic (SODm) capabilities. The crystal structure of the seven-coordinate OMe-substituted Mn-pyane complex was obtained. The synthesized complexes will serve for future investigations related to an effect of complex redox potentials on their mechanistic behavior within SOD catalysis.

Ruthenium(II) sensitizers with heteroleptic tridentate chelates for dye-sensitized solar cells

Chou, Chun-Cheng,Wu, Kuan-Lin,Chi, Yun,Hu, Wei-Ping,Yu, Shuchun Joyce,Lee, Gene-Hsiang,Lin, Chi-Li,Chou, Pi-Tai

, p. 2054 - 2058 (2011/04/23)

Two new for Ru: Unprecedented RuII sensitizers are coordinated by two tridentate ligands, a tricarboxyterpyridine, and a dianionic bis(pyrazolyl)pyridine derivative with an extended π-conjugated auxochrome (see picture, Rumagenta, Nblue, Ored, Fgreen, Syellow, Cgray). This new generation of thiocyanate-free RuII sensitizers offers solar conversion efficiency in dye-sensitized solar cells up to I·=10.7 %.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 195967-10-3