31872-65-8 | 3-Bromo-4-hydroxy-5-nitropyridine

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$8.00	$6.00
1g	95%	in stock	$12.00	$9.00
5g	95%	in stock	$24.00	$17.00

Description

• Catalog Number: AB64462
• Chemical Name: 3-Bromo-4-hydroxy-5-nitropyridine
• CAS Number: 31872-65-8
• Molecular Formula: C5H3BrN2O3
• Molecular Weight: 218.9929
• MDL Number: MFCD08692339
• SMILES: [O-][N+](=O)c1cncc(c1O)Br

Computed Properties

• Complexity: 276
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

3-Bromo-5-nitropyridin-4-ol, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, it serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromo and nitro functional groups enable facile manipulation through different chemical reactions, allowing for the introduction of diverse functionality into target molecules.One common application of 3-Bromo-5-nitropyridin-4-ol is as a precursor for the synthesis of heterocyclic compounds, which are essential structural motifs found in many biologically active molecules. By incorporating this compound into the synthetic route, chemists can access a wide range of heterocyclic derivatives with potential applications in drug discovery and materials science. Additionally, the presence of the nitro group offers the possibility of further functionalization through reduction or substitution reactions, expanding the scope of synthetic pathways that can be explored.Furthermore, the unique reactivity of 3-Bromo-5-nitropyridin-4-ol makes it a valuable tool for the construction of complex molecular architectures through cascade reactions or multistep syntheses. Its ability to participate in various cross-coupling reactions, cyclization processes, and functional group transformations allows for efficient and selective bond formation, crucial for the development of new chemical entities with desired properties.Overall, 3-Bromo-5-nitropyridin-4-ol plays a crucial role in modern organic synthesis as a versatile reagent for the construction of diverse chemical structures with important applications in the pharmaceutical, agricultural, and materials industries.