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898746-91-3

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898746-91-3 Usage

General Description

6-Bromo-4-indole carboxylic acid is a chemical compound with the molecular formula C9H6BrNO2. It is a derivative of indole carboxylic acid, and it contains a bromine atom at the 6th position of the indole ring. 6-BROMO-4-INDOLE CARBOXYLIC ACID is commonly used in the synthesis of various pharmaceuticals and organic compounds. It is known for its potential antibacterial and antifungal properties, making it a valuable building block for the development of new drugs. Additionally, it has also been investigated for its potential use in the treatment of certain types of cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 898746-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,7,4 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 898746-91:
(8*8)+(7*9)+(6*8)+(5*7)+(4*4)+(3*6)+(2*9)+(1*1)=263
263 % 10 = 3
So 898746-91-3 is a valid CAS Registry Number.

898746-91-3SDS

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 6-Bromo-1H-indole-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-bromo-1H-indole-4-carboxylic acid

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:898746-91-3 SDS

898746-91-3Upstream product

898746-91-3Downstream Products

898746-91-3Relevant articles and documents

Development and Scale-up of Continuous Electrocatalytic Hydrogenation of Functionalized Nitro Arenes, Nitriles, and Unsaturated Aldehydes

Egbert, Jonathan D.,Thomsen, Edwin C.,O'Neill-Slawecki, Stacy A.,Mans, Douglas M.,Leitch, David C.,Edwards, Lee J.,Wade, Charles E.,Weber, Robert S.

, p. 1803 - 1812 (2019)

Electrolysis flow reactors based on the filter-press architecture of redox flow batteries have proven to be effective and scalable toward the production of commercially relevant, pharmaceutical quantities of anilines (>500 kg/year) from halogen-, hydroxyl-, and carbonyl-substituted nitroarenes. Turbulent flow through the carbon felts on which the catalysts were supported facilitated scaling toward production levels because it conferred on the reactors scale-independent, plug flow-like residence time distributions and high mass transfer coefficients. Equipping the cells with microreference electrodes made it possible to transfer reaction conditions first developed in batch systems to the continuous flow reactors. The catalysts prepared by incipient wetness impregnation of metal salts into lightly oxidized carbon felt supports were readily generalizable.

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