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1187386-12-4

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1187386-12-4 Usage

General Description

6-Bromo-2-methoxy-4-methylquinoline is a specialized chemical compound that belongs to the family of Quinolines and Isoquinolines. This derivative of quinoline possesses multiple functional groups such as bromo, methoxy, and methyl groups. The presence of these groups can significantly influence the chemical's properties and reactivity. These types of compounds are often used in various sectors of chemistry, including pharmaceutical and medicinal chemistry, where they contribute to the synthesis of new drugs and substances. Detailed information about its toxicity, safety hazards, or environmental effects may not be readily available due to its specificity and specialized use.

Check Digit Verification of cas no

The CAS Registry Mumber 1187386-12-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,3,8 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1187386-12:
(9*1)+(8*1)+(7*8)+(6*7)+(5*3)+(4*8)+(3*6)+(2*1)+(1*2)=184
184 % 10 = 4
So 1187386-12-4 is a valid CAS Registry Number.

1187386-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-2-methoxy-4-methylquinoline

1.2 Other means of identification

Product number -
Other names 6-bromo-4-methyl-2-methoxyquinoline

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:1187386-12-4 SDS

1187386-12-4Relevant 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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