126350-18-3

Basic information

• Product Name: 6,8-DICHLORO-2H-CHROMENE-3-CARBALDEHYDE
• Synonyms: 6,8-DICHLORO-2H-CHROMENE-3-CARBALDEHYDE;2H-1-Benzopyran-3-carboxaldehyde,6,8-dichloro-
• CAS NO: 126350-18-3
• Molecular Formula: C10H6Cl2O2
• Molecular Weight: 229.06
• Mol File: 126350-18-3.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6,8-DICHLORO-2H-CHROMENE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6,8-DICHLORO-2H-CHROMENE-3-CARBALDEHYDE(126350-18-3)
• EPA Substance Registry System: 6,8-DICHLORO-2H-CHROMENE-3-CARBALDEHYDE(126350-18-3)

Safety Data

• Hazard Codes: Xi,N
• Statements: 36/37/38-51/53
• Hazardous Substances Data: 126350-18-3(Hazardous Substances Data)

Usage

General Description

6,8-Dichloro-2H-chromene-3-carbaldehyde is a synthetic compound that belongs to the family of Chromenes. It exhibits a structural arrangement consisting of a benzene ring fused to a pyran ring, which is further substituted by two chloro groups at positions 6 and 8 and an aldehyde group at position 3. As it is a relatively specific chemical entity, it is primarily used in scientific research. Due to its chlorinated and aldehyde properties, it may potentially exercise a certain degree of reactivity and caution may be necessary when handling or storing. Detailed information about its toxicity, environmental impact, and specific uses is limited and would require further research.

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Relevant articles and documents

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

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

Synthesis and characterisation of 5-(6-substituted phenyl-2H-chromen-3-yl) oxazole derivatives

Here we demonstrate the synthesis of various derivatives of 5-(6-substituted phenyl-2H-chromen-3-yl)- oxazoles 5(a-k) by using Suzuki coupling conditions with different substituted boronic acids and obtained 23-57 % yields. We also synthesised various derivatives of the 5-(substituted 2H-chromen-3-yl)-oxazoles 3(a-j) mediated by TOSMIC as a reagent and achieved 58-70 % yield.