201420-31-7

Basic information

• Product Name: 6-BROMO-4-CHLOROQUINOLINE-3-CARBALDEHYDE
• Synonyms: 6-BROMO-4-CHLOROQUINOLINE-3-CARBALDEHYDE;6-bromo-4-chloro-3-Quinolinecarboxaldehyde
• CAS NO: 201420-31-7
• Molecular Formula: C10H5BrClNO
• Molecular Weight: 270.5098
• Product Categories: Quinoline&Isoquinoline
• Mol File: 201420-31-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 378.6±37.0 °C(Predicted)
• Appearance: /
• Density: 1.727±0.06 g/cm3(Predicted)
• PKA: 1.13±0.27(Predicted)
• CAS DataBase Reference: 6-BROMO-4-CHLOROQUINOLINE-3-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-BROMO-4-CHLOROQUINOLINE-3-CARBALDEHYDE(201420-31-7)
• EPA Substance Registry System: 6-BROMO-4-CHLOROQUINOLINE-3-CARBALDEHYDE(201420-31-7)

Safety Data

• Hazardous Substances Data: 201420-31-7(Hazardous Substances Data)

Usage

General Description

6-Bromo-4-chloroquinoline-3-carbaldehyde is a chemical compound with the molecular formula C10H5BrClNO. It is an aldehyde derivative of the quinoline class of compounds, which are known for their diverse range of biological activities. This particular compound is used in the synthesis of pharmaceuticals and agrochemicals, including potential antimalarial and antiviral agents. It is also used as a reagent in chemical reactions and as a building block for the synthesis of other biologically active compounds. Its unique structure and reactivity make it a valuable tool in the field of medicinal and synthetic chemistry.

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Relevant articles and documents

Novel D-π-A organic dyes for DSSCs based on dibenzo[b,h][1,6]naphthyridine as a π-bridge

A new series of D-π-A organic dyes bearing fused dibenzo[b,h] [1,6]naphthyridine as the conjugated π-bridge, a cyanoacrylic acid moiety as the electron acceptor/anchoring group and different electron donor groups such as trimethoxy (5a), methoxy (5b) and

Synthesis of (2-Aminophenyl)(naphthalen-2-yl)methanones via Intramolecular Rearrangement of (E)-3-Styrylquinolin-4(1 H)-ones under Irradiation with 365 nm UV Light

A highly efficient and environmentally friendly synthesis of (2-aminophenyl)(naphthalen-2-yl)methanones was developed. The (2-aminophenyl)(naphthalen-2-yl)methanone derivatives were obtained in high yields (up to 96%) by the irradiation of (E)-3-styrylquinolin-4(1 H)-ones in EtOH-H 2 O (7:1) with UV light (365 nm) at room temperature under Ar atmosphere. The demonstrated photoinduced intramolecular rearrangement has advantages over other transition-metal-catalyzed reactions, e.g. no requirement of additives, green solvent, broad substrate scope, and high atom efficiency.

Fused ring compound and preparation method, application and intermediate compound thereof

The invention relates to a fused ring compound and a preparation method, application and intermediate compound thereof. The fused ring compound can be used as an inhibitor of phosphatidylinositol 3-kinase.