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41320-96-1

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41320-96-1 Usage

General Description

3,4-Dibromoquinoline is a chemical compound with the molecular formula C9H5Br2N. It is a yellowish-brown solid that is insoluble in water but soluble in organic solvents. 3,4-Dibromoquinoline is used in the pharmaceutical and agrochemical industries as an intermediate in the synthesis of various compounds. It has been studied for its potential antimalarial and anticancer properties, and has also been used in the development of fluorescent dyes and organic light-emitting diodes. The compound is considered to be moderately toxic, and exposure to 3,4-Dibromoquinoline should be minimized to prevent adverse health effects.

Check Digit Verification of cas no

The CAS Registry Mumber 41320-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41320-96:
(7*4)+(6*1)+(5*3)+(4*2)+(3*0)+(2*9)+(1*6)=81
81 % 10 = 1
So 41320-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H5Br2N/c10-7-5-12-8-4-2-1-3-6(8)9(7)11/h1-5H

41320-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-DIBROMOQUINOLINE

1.2 Other means of identification

Product number -
Other names 3,4-Dibrom-chinolin

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:41320-96-1 SDS

41320-96-1Relevant articles and documents

Studies of one-pot double couplings on dibromoquinolines

Piala, Alexander,Mayi, Diyar,Handy, Scott T.

, p. 4147 - 4154 (2011/07/08)

In a series of studies, the regioselectivity of Suzuki couplings of dibromoquinolines has been investigated. In general, it is much harder to achieve high levels of regioselectivity in these systems compared to many of the other dibromoheteroaromatics that have been studied. Useful levels of selectivity could be achieved for both a 5,7-dibromoquinoline as well as 3,4-dibromoquinoline. Double Suzuki couplings could also be achieved on these two compounds.

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