885267-41-4

Basic information

• Product Name: 5-BROMOQUINOLINE-8-CARBALDEHYDE
• Synonyms: 5-BROMOQUINOLINE-8-CARBALDEHYDE;8-Quinolinecarboxaldehyde, 5-broMo-;5-Bromo-8-formylquinoline, 5-Bromo-8-formyl-1-azanaphthalene
• CAS NO: 885267-41-4
• Molecular Formula: C₁₀H₆BrNO
• Molecular Weight: 236.06
• Product Categories: Organohalides;Quinoline
• Mol File: 885267-41-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 374.6±27.0 °C(Predicted)
• Appearance: /
• Density: 1.632±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 2.37±0.29(Predicted)
• CAS DataBase Reference: 5-BROMOQUINOLINE-8-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMOQUINOLINE-8-CARBALDEHYDE(885267-41-4)
• EPA Substance Registry System: 5-BROMOQUINOLINE-8-CARBALDEHYDE(885267-41-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 885267-41-4(Hazardous Substances Data)

Usage

General Description

5-Bromoquinoline-8-carbaldehyde is a chemical compound with the molecular formula C10H6BrNO. It is a derivative of quinoline and is commonly used as a precursor in the synthesis of various pharmaceuticals and organic compounds. This chemical is known for its aromatic properties and is often utilized in organic synthesis and medicinal chemistry. It is primarily used as a building block in the production of heterocyclic compounds and is also used in the development of fluorescent probes for bioimaging applications. 5-Bromoquinoline-8-carbaldehyde is an important intermediate in the production of various pharmaceutical drugs and organic molecules, making it a valuable compound in the chemical industry.

Upstream product

• 39478-78-9 5-bromo-2-methylaniline 
• 74316-55-5 5-bromo-8-methyl-quinoline 
• 1309959-33-8 5-bromo-8-(dibromomethyl)quinoline 
• 611-32-5 8-methylquinoline 

Downstream Products

• 1093281-24-3 5-(4-methoxyphenyl)quinoline-8-carbaldehyde 
• 1403380-09-5 5-[3-fluoro-4-(3-phenylpropyl)phenyl]quinoline-8-carbaldehyde 
• 1402908-80-8 5-(6-phenylhex-1-yn-1-yl)quinoline-8-carbaldehyde 
• 1445781-87-2 (S)-5-((1-(3-fluorophenyl)-2-(methylamino)ethyl)amino)quinoline-8-carboxamide 
• 1445781-88-3 (S)-5-{1-(3-fluoro-phenyl)-2-[methyl-(4-nitro-benzenesulfonyl)-amino]-ethylamino}-quinoline-8-carboxylic acid methyl ester 
• 1445781-89-4 (S)-5-{1-(3-fluoro-phenyl)-2-[methyl-(4-nitro-benzenesulfonyl)-amino]-ethylamino}-quinoline-8-carboxamide 
• 1445781-45-2 methyl 5-bromoquinoline-8-carboxylate 
• 1590378-61-2 5-(4-phenylbutyl)-3{8-[(tetrahydro-2H-pyran-2-yloxy)methyl]quinoline-5-yl}-1,2,4-oxadiazole 
• 1590378-65-6 {5-[5-(4-phenylbutyl)-1,2,4-oxadiazol-3-yl]quinoline-8-yl}methanol 
• 1590378-69-0 5-[5-(4-phenylbutyl)-1,2,4-oxadiazol-3-yl]quinoline-8-carbaldehyde 
• 507476-70-2 5-bromo-quinoline-8-carbonitrile 

Relevant articles and documents

Rhodium(III)-Catalyzed Direct Coupling of Quinoline-8-Carbaldehydes with (Het)Arylboronic Acids for the Synthesis of 8-Aryloylquinolines

Herein, we describe a method for the synthesis of aryl-(het)aryl ketones by Rh(III)-catalyzed direct coupling between quinoline-8-carbaldehydes and (het)arylboronic acids. The method has a broad substrate scope, a high functional group tolerance, and uses

NOVEL HETEROCYCLIC CARBOXAMIDES AS MODULATORS OF KINASE ACTIVITY

The invention provides novel heterocyclic carboxamide compounds compounds according to Formula (I) their manufacture and use for the treatment of hyperproliferative diseases, such as cancer.

INSECTICIDAL COMPOUNDS BASED ON ISOXAZOLINE DERIVATIVES

The present invention relates to compounds of formula (I): Wherein A1, A2, A3, A4, G1, L, Y1, Y2, Y3, Y4, R1, R2, R3 and R