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500127-41-3

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500127-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 500127-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,1,2 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 500127-41:
(8*5)+(7*0)+(6*0)+(5*1)+(4*2)+(3*7)+(2*4)+(1*1)=83
83 % 10 = 3
So 500127-41-3 is a valid CAS Registry Number.

500127-41-3SDS

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 4-chloro-6-(4-methoxyphenyl)quinoline

1.2 Other means of identification

Product number -
Other names -

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:500127-41-3 SDS

500127-41-3Downstream Products

500127-41-3Relevant articles and documents

Successive substitution of halogen atoms in 4,6-dihaloquinolines in palladium-catalyzed reactions with amines and arylboronic acids

Beletskaya,Tsvetkov,Tsvetkov,Latyshev,Lukashev

, p. 215 - 219 (2005)

A procedure was developed for the synthesis of 4,6-diamino- and 4,6- or 6,4-arylaminoquinolines by palladium-catalyzed C-N- and/or C-C-cross-coupling of 6-bromo-4-chloroquinoline.

The successive substitution of halogens in 4-chloro-6-iodoquinoline by aryl groups in cross-coupling reactions with arylboronic acids

Tsvetkov, Alexey V.,Latyshev, Gennadij V.,Lukashev, Nikolai V.,Beletskaya, Irina P.

, p. 7267 - 7270 (2007/10/03)

The conditions for selective stepwise substitution of iodine and chlorine atoms in 4-chloro-6-iodoquinoline which allow the synthesis of the corresponding diarylquinolines with different aryl groups in the 4- and 6-positions, in a one-pot procedure, in hi

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