1196155-68-6 | 6-bromoquinoline-3-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$50.00	$35.00
1g	97%	in stock	$60.00	$42.00
5g	97%	in stock	$299.00	$210.00
10g	97%	in stock	$597.00	$418.00

Description

• Catalog Number: AA32622
• Chemical Name: 6-bromoquinoline-3-carbaldehyde
• CAS Number: 1196155-68-6
• Molecular Formula: C10H6BrNO
• Molecular Weight: 236.0647
• MDL Number: MFCD13190233
• SMILES: O=Cc1cnc2c(c1)cc(cc2)Br

Computed Properties

• Complexity: 197
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

6-Bromoquinoline-3-carbaldehyde, a valuable chemical compound in the field of organic synthesis, serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials. Its versatile nature allows it to participate in a range of important chemical reactions, making it a sought-after reagent in the laboratory.One of the key applications of 6-Bromoquinoline-3-carbaldehyde is its role as a precursor in the synthesis of quinoline-based molecules. By utilizing this compound, chemists can introduce specific functional groups or structural motifs onto the quinoline scaffold, leading to the development of new drug candidates or complex organic compounds. This versatile aldehyde is particularly valuable in the modification of quinoline derivatives for targeted biological activities, allowing for the exploration of diverse chemical space in drug discovery efforts.Furthermore, 6-Bromoquinoline-3-carbaldehyde can be employed in tandem with various coupling reactions, such as Suzuki-Miyaura cross-coupling or Heck reactions, to form carbon-carbon bonds and construct more intricate molecules. Its ability to serve as a key intermediate in the synthesis of heterocyclic compounds and biologically active molecules underscores its importance in modern organic chemistry research.In summary, the application of 6-Bromoquinoline-3-carbaldehyde in chemical synthesis extends beyond its basic chemical properties, offering chemists a powerful tool for the creation of novel compounds with potential therapeutic or practical applications. Its versatility and reactivity make it a valuable asset in the quest for new chemical entities and innovative materials.