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532392-88-4

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532392-88-4 Usage

General Description

2,4-Dibromo-3-quinolinemethanol is a chemical compound that contains two bromine atoms and a quinoline ring structure. It is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 2,4-Dibromo-3-quinolinemethanol has been found to exhibit antibacterial and antifungal properties, making it valuable in the development of new drugs and fungicides. It is also used as a building block for the production of other chemical compounds, due to its versatile reactivity. However, it is important to handle this chemical with caution as it can be harmful if ingested, inhaled, or absorbed through the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 532392-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,2,3,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 532392-88:
(8*5)+(7*3)+(6*2)+(5*3)+(4*9)+(3*2)+(2*8)+(1*8)=154
154 % 10 = 4
So 532392-88-4 is a valid CAS Registry Number.

532392-88-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,4-dibromoquinolin-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 2,4-Dibromo-3-quinolinemethanol

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:532392-88-4 SDS

532392-88-4Downstream Products

532392-88-4Relevant articles and documents

Regioselective Sonogashira couplings of 2,4-dibromoquinolines. A correction

Nolan, Jason M.,Comins, Daniel L.

, p. 3736 - 3738 (2003)

Heteronuclear multiple bond correlation (HMBC) was used to determine the regiochemical outcome of palladium-catalyzed carbon-carbon bond formation between 2,4-dibromoquinolines and terminal acetylenes. The observed regioselectivity of these coupling react

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