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84741-86-6

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84741-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84741-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,4 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84741-86:
(7*8)+(6*4)+(5*7)+(4*4)+(3*1)+(2*8)+(1*6)=156
156 % 10 = 6
So 84741-86-6 is a valid CAS Registry Number.

84741-86-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Quinoline-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names Chinolin-3-carbonylchlorid

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:84741-86-6 SDS

84741-86-6Relevant articles and documents

Crystal structure, Hirshfeld surface analysis and DFT studies of N-(4-acetylphenyl)quinoline-3-carboxamide

Brito, Iván,Cisterna, Jonathan,Ferrer, Karoll,Gutiérrez, Margarita,Osorio, Edison,Polo-Cuadrado, Efraín

, (2021/08/05)

Crystalline organic compound, N-(4-acetylphenyl)quinoline-3-carboxamide (4) was readily prepared using our previously reported experimental procedure by the reaction of quinoline-3-carboxylic acid (1) with thionyl chloride to generate the acid chloride in

Heterocyclic compound and preparation and application thereof

-

Paragraph 0222-0224, (2020/07/24)

The invention relates to bromodomain inhibitors, and provides a compound represented by a general formula I, a pharmaceutically acceptable salt, an enantiomer, a diastereoisomer, an atropisomer, a racemate, a polymorph, a solvate or an isotope-labeled compound (including deuterium substitution) thereof, a preparation method thereof, a pharmaceutical composition containing the same, and applicationthereof in pharmacy.

Ultrasound-assisted synthesis of novel chalcone, heterochalcone and bis-chalcone derivatives and the evaluation of their antioxidant properties and as acetylcholinesterase inhibitors

Polo, Efraín,Ibarra-Arellano,Prent-Pe?aloza, Luis,Morales-Bayuelo, Alejandro,Henao, José,Galdámez, Antonio,Gutiérrez, Margarita

, (2019/07/08)

The chalcone and bis-chalcone derivatives have been synthesized under sonication conditions via Claisen-Schmidt condensation with KOH in ethanol at room temperature (20–89%). The structures were established on the basis of NMR, IR, Single-crystal XRD, and

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