1172085-67-4 | 5-bromo-[1,2,4]triazolo[4,3-a]pyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$66.00	$46.00
250mg	95%	in stock	$113.00	$79.00
500mg	95%	in stock	$164.00	$115.00
1g	95%	in stock	$249.00	$174.00
5g	95%	in stock	$808.00	$566.00
10g	95%	in stock	$1,317.00	$922.00
25g	95%	in stock	$2,623.00	$1,836.00

Description

• Catalog Number: AA17843
• Chemical Name: 5-bromo-[1,2,4]triazolo[4,3-a]pyridine
• CAS Number: 1172085-67-4
• Molecular Formula: C6H4BrN3
• Molecular Weight: 198.0201
• MDL Number: MFCD11043995
• SMILES: Brc1cccc2n1cnn2

Computed Properties

• Complexity: 130
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 2.2

Upstream Synthesis Route

5-Bromo-[1,2,4]triazolo[4,3-a]pyridine, a versatile building block in chemical synthesis, serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and functional materials. With its unique structure and reactivity, this compound plays a crucial role in the development of novel compounds with diverse applications.In organic synthesis, 5-Bromo-[1,2,4]triazolo[4,3-a]pyridine can be utilized as a key component in the construction of heterocyclic frameworks through various reactions such as functional group transformations, cross-coupling reactions, and cyclization processes. Its ability to participate in diverse chemical transformations makes it a valuable tool for the creation of bioactive molecules and complex organic structures.Furthermore, 5-Bromo-[1,2,4]triazolo[4,3-a]pyridine's unique scaffold provides opportunities for the design and synthesis of new materials with specific properties, such as fluorescent dyes, sensors, and advanced coordination complexes. By incorporating this versatile building block into molecular architectures, researchers can tailor the properties of the resulting materials for a wide range of applications in fields such as materials science and chemical biology.Overall, the strategic placement of the bromo-substituent on the triazolopyridine scaffold enhances the compound's utility in chemical synthesis, allowing for the efficient preparation of diverse molecular structures with potential applications in various industries.