1017412-53-1 | 5-Bromoquinoline-2-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$41.00	$29.00
250mg	97%	in stock	$49.00	$35.00
1g	97%	in stock	$70.00	$49.00
5g	97%	in stock	$276.00	$193.00
25g	97%	in stock	$1,319.00	$923.00

Description

• Catalog Number: AA06749
• Chemical Name: 5-Bromoquinoline-2-carboxylic acid
• CAS Number: 1017412-53-1
• Molecular Formula: C10H6BrNO2
• Molecular Weight: 252.06414000000004
• MDL Number: MFCD19689976
• SMILES: OC(=O)c1ccc2c(n1)cccc2Br

Computed Properties

• Complexity: 234
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.7

Upstream Synthesis Route

5-Bromoquinoline-2-carboxylic acid is a versatile chemical compound that finds wide application in chemical synthesis processes, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key building block for the synthesis of various biologically active molecules due to its unique structural features and reactivity.In chemical synthesis, 5-Bromoquinoline-2-carboxylic acid can be utilized as a precursor in the preparation of quinoline-based drugs, agrochemicals, and advanced materials. Its bromo substituent allows for further derivatization through various cross-coupling reactions, such as Suzuki-Miyaura coupling or Negishi coupling, enabling the introduction of diverse functional groups.Additionally, the carboxylic acid group in 5-Bromoquinoline-2-carboxylic acid can participate in amide formation reactions, leading to the synthesis of amide-containing compounds with potential biological activities. Furthermore, this compound can undergo cyclization reactions to form fused heterocyclic structures, which are commonly found in pharmaceuticals and natural products.Overall, the strategic incorporation of 5-Bromoquinoline-2-carboxylic acid in chemical synthesis enables the efficient construction of complex molecules with desired pharmacological or agricultural properties. Its utility lies in its ability to serve as a key intermediate for the synthesis of diverse functionalized quinoline derivatives, making it a valuable tool for organic chemists and drug discovery researchers.