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6-Chloro-3-Fluoro-2-hydroxyquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

834883-95-3

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834883-95-3 Usage

Molecular weight

191.59 g/mol

Structure

Chlorinated and fluorinated derivative of quinoline

Functional groups

Hydroxyl group attached to the carbon atom in the 2 position

Uses

Synthesis of pharmaceuticals and agrochemicals
Antimicrobial and antiviral activity
Building block in the production of pharmaceuticals, dyes, and other organic compounds

Potential applications

Research and development in medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 834883-95-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,4,8,8 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 834883-95:
(8*8)+(7*3)+(6*4)+(5*8)+(4*8)+(3*3)+(2*9)+(1*5)=213
213 % 10 = 3
So 834883-95-3 is a valid CAS Registry Number.

834883-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-3-fluoro-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names 6-chloro-3-fluoroquinol-2(1H)-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:834883-95-3 SDS

834883-95-3Upstream product

834883-95-3Relevant academic research and scientific papers

Metalation/functionalization sequences applied to 2-bromo-3- fluoroquinolines

Ondi, Levente,Volle, Jean-No?l,Schlosser, Manfred

, p. 717 - 725 (2007/10/03)

Mono- and disubstituted 2-bromo-3-fluoroquinolines 3 are readily accessible. They can be converted into the 3-fluoroquinoline-2-carboxylic acids 5 by consecutive halogen/metal permutation and into the 2-bromo-3- fluoroquinoline-4-carboxylic acids 6 by con

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