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6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE is a chemical compound with the molecular formula C10H6Br2O2. It is a derivative of chromene and contains two bromine atoms and an aldehyde functional group. 6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE is commonly used in organic synthesis and medicinal chemistry as a building block for the production of various pharmaceuticals and biologically active compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of heterocyclic compounds and complex organic molecules. Additionally, it has been identified as a potential inhibitor of certain enzymes and has shown promising anti-cancer and anti-inflammatory properties in preliminary studies.

885271-27-2

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885271-27-2 Usage

Uses

Used in Pharmaceutical Industry:
6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE is used as a building block for the production of various pharmaceuticals and biologically active compounds. Its unique structure and reactivity make it a valuable intermediate in the synthesis of heterocyclic compounds and complex organic molecules.
Used in Organic Synthesis:
6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE is used as a key intermediate in the synthesis of heterocyclic compounds and complex organic molecules, contributing to the development of new chemical entities with potential applications in various fields.
Used in Enzyme Inhibition:
6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE has been identified as a potential inhibitor of certain enzymes, making it a candidate for further research and development in the area of enzyme-targeted therapies.
Used in Anti-Cancer Research:
6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE has shown promising anti-cancer properties in preliminary studies, indicating its potential use in the development of novel cancer treatments.
Used in Anti-Inflammatory Research:
6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE has demonstrated anti-inflammatory properties, suggesting its potential application in the development of new anti-inflammatory drugs.

Check Digit Verification of cas no

The CAS Registry Mumber 885271-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 1 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 885271-27:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*1)+(2*2)+(1*7)=202
202 % 10 = 2
So 885271-27-2 is a valid CAS Registry Number.

885271-27-2SDS

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 6,8-DIBROMO-2H-CHROMENE-3-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyran-3-carboxaldehyde,6,8-dibromo

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:885271-27-2 SDS

885271-27-2Downstream Products

885271-27-2Relevant academic research and scientific papers

Design, one-pot synthesis, molecular docking study, and antibacterial evaluation of novel 2H-chromene based imidazo[1,2-a]pyridine derivatives as potent peptide deformylase inhibitors

Jena, Subhrakant,Mishra, Nilima Priyadarsini,Mohapatra, Seetaram,Nayak, Sabita,Padhy, Rabindra Nath,Raiguru, Bishnu Prasad,Sahoo, Chita Ranjan

, (2021/08/09)

An efficient, environmentally friendly, one-pot three-component synthesis of a series of 2H-chromene-based imidazo[1,2-a]pyridines had been designed and were synthesized. This protocol was developed by the reaction of substituted 2H-chromene aldehydes and

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