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AKOS BC-0237, also known as 5-chloro-N-(2,4-dimethylphenyl)-2-hydroxybenzenesulfonamide, is a chemical compound with the molecular formula C10H10ClNO5S. It is a white to off-white powder with a molecular weight of 281.70 g/mol. AKOS BC-0237 is used in various industrial and pharmaceutical applications and is not listed as a hazardous substance by the OSHA Hazard Communication Standard (29 CFR 1910.1200). It has no known toxicological properties, but it is important to handle and store it in accordance with safe laboratory practices and local regulations to minimize any potential risks associated with its use.

51641-22-6

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51641-22-6 Usage

Uses

Used in Pharmaceutical Industry:
AKOS BC-0237 is used as an active pharmaceutical ingredient for the development of medications targeting various health conditions. Its specific application reason is not provided in the materials.
Used in Industrial Applications:
AKOS BC-0237 is used as a chemical intermediate or component in the synthesis of other compounds for various industrial purposes. The exact application reason is not specified in the materials.

Check Digit Verification of cas no

The CAS Registry Mumber 51641-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,4 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51641-22:
(7*5)+(6*1)+(5*6)+(4*4)+(3*1)+(2*2)+(1*2)=96
96 % 10 = 6
So 51641-22-6 is a valid CAS Registry Number.

51641-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydro-1H-isoquinolin-4-one

1.2 Other means of identification

Product number -
Other names 1,2,3,4-TETRAHYDROISOQUINOLIN-4-ONE

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:51641-22-6 SDS

51641-22-6Downstream Products

51641-22-6Relevant academic research and scientific papers

A Cu-Doped ZIF-8 metal organic framework as a heterogeneous solid catalyst for aerobic oxidation of benzylic hydrocarbons

Nagarjun, Nagarathinam,Dhakshinamoorthy, Amarajothi

, p. 18702 - 18712 (2019)

Mixed-metal metal organic frameworks have received considerable attention in recent years and it has been shown that the activity of the parent metal organic framework (MOF) is often enhanced upon doping with external metal ions within the framework. In this context, Cu2+ ions with different loadings were incorporated within the ZIF-8 framework to obtain a series of Cu-doped ZIF-8 materials and their activity was examined in the aerobic oxidation of hydrocarbons. The as-synthesized Cu-doped solids were characterized by powder X-ray diffraction (XRD), ultraviolet diffuse reflectance spectroscopy (UV-DRS), scanning electron microscopy (SEM), Fourier Transform infrared (FT-IR), electron paramagnetic resonance (EPR) and inductively coupled plasma (ICP) analysis. The experimental results revealed that the activity of Cu-doped ZIF-8 is much higher than that of the parent ZIF-8 in all the tested substrates at 120 °C. Furthermore, the activity of the Cu-doped ZIF-8 with the highest Cu loading was eight fold higher than that of the parent ZIF-8 in the aerobic oxidation of cyclooctane (1) at 120 °C with more than 80% selectivity to the corresponding cyclooctanol/cyclooctanone (ol/one) mixture. Cu-doped ZIF-8 was reused two times with no significant drop in its activity under identical conditions. Furthermore, comparison of the two times reused solid with that of the fresh solid by powder XRD and SEM analysis revealed identical structural integrity and morphology, respectively during the oxidation reactions.

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