29681-44-5 | Methyl 5-bromonicotinate

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$13.00	$9.00
100g	98%	in stock	$28.00	$19.00

Description

• Catalog Number: AB38596
• Chemical Name: Methyl 5-bromonicotinate
• CAS Number: 29681-44-5
• Molecular Formula: C7H6BrNO2
• Molecular Weight: 216.032
• MDL Number: MFCD00173668
• SMILES: COC(=O)c1cncc(c1)Br

Computed Properties

• Complexity: 151
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 1.4

Upstream Synthesis Route

Methyl 5-bromonicotinate is a versatile compound widely used in organic synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, Methyl 5-bromonicotinate can act as a valuable intermediate for the construction of complex organic molecules. Its bromine functional group allows for selective transformations, such as substitution reactions, leading to the introduction of new functional groups or structural modifications. This enables chemists to tailor the molecular structure of the desired compound with precision.Furthermore, Methyl 5-bromonicotinate is commonly employed in the synthesis of heterocyclic compounds. Its nicotinate moiety provides a versatile platform for the formation of diverse nitrogen-containing ring systems, which are prevalent in many biologically active molecules. By incorporating this compound into a synthetic pathway, chemists can access a wide range of heterocycles with potential applications in drug discovery and material science.Overall, Methyl 5-bromonicotinate plays a crucial role in advancing the field of organic synthesis by enabling the efficient construction of complex molecules with specific functionalities. Its diverse applications make it a valuable tool for chemists seeking to design and access novel compounds for various industrial and research purposes.

Literature

• The synthesis of 5-substituted ring E analogs of methyllycaconitine via the Suzuki-Miyaura cross-coupling reaction.

  Bioorganic & medicinal chemistry 20080401