120277-70-5

Basic information

• Product Name: 3-BROMOMETHYLQUINOLINE
• Synonyms: 3-BROMOMETHYLQUINOLINE
• CAS NO: 120277-70-5
• Molecular Formula: C₁₀H₈BrN
• Molecular Weight: 222.09
• Mol File: 120277-70-5.mol
• Article Data: 4

Chemical Properties

• Melting Point: 54.5 °C
• Boiling Point: 317.5±17.0 °C(Predicted)
• Appearance: /
• Density: 1.518±0.06 g/cm3(Predicted)
• PKA: 3.99±0.11(Predicted)
• CAS DataBase Reference: 3-BROMOMETHYLQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMOMETHYLQUINOLINE(120277-70-5)
• EPA Substance Registry System: 3-BROMOMETHYLQUINOLINE(120277-70-5)

Safety Data

• Hazardous Substances Data: 120277-70-5(Hazardous Substances Data)

Usage

General Description

3-Bromomethylquinoline, also known as Quinoline, 3-(bromomethyl)-, is a chemical compound with the molecular formula C10H8BrN. It is typically used in the field of organic synthesis, notably in the production of pharmaceuticals and agrochemicals. It is a brown crystalline solid and is sensitive to light. It is also considered to be harmful if swallowed or comes into contact with skin and eyes. This bromomethylquinoline must be handled with care and used only by those experienced in handling hazardous materials.

Upstream product

• 13669-51-7 3-Hydroxymethylquinoline 
• 13669-42-6 3-quinolylcarboxaldehyde 
• 612-58-8 3-methylquinoline 

Downstream Products

• 7521-70-2 3-(aminomethyl)quinoline 
• 6480-68-8 quinoline-3-carboxylic acid 
• 1001055-28-2 C₂₈H₃₁N₅O₄ 
• 1001054-95-0 C₂₇H₃₀N₄O₃ 

Relevant articles and documents

COMPOUNDS AND METHODS FOR TREATMENT OF CANCER BY INHIBITING ATG4B AND BLOCKING AUTOPHAGY

ATG4B inhibitor compounds, compositions that include the compounds, and methods for using the compounds and compositions in the treatment of cancer by inhibiting ATG4B and/or blocking autophagy.

Design, synthesis, and biological activities of novel 2-cyanoacrylates containing oxazole, oxadiazole, or quinoline moieties

A series of novel 2-cyanoacrylates containing an oxazole, oxadiazole, or quinoline moiety were designed and synthesized, and their structures were characterized by 1H NMR and elemental analysis (or high-resolution mass spectrometry). Their herbicidal activities against four weeds were evaluated, and the result indicated that some of the title compounds showed excellent herbicidal activities against rape and amaranth pigweed in postemergence treatment at a dose of 375 g/ha. Furthermore, most of these cyanoacrylates exhibited interesting plant growth regulatory activities.