1211589-41-1 | Methyl 5-bromo-2-(trifluoromethyl)pyridine-4-carboxylate

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$28.00	$19.00
250mg	97%	in stock	$52.00	$36.00
1g	97%	in stock	$60.00	$42.00
5g	97%	in stock	$240.00	$168.00
100g	97%	in stock	$4,488.00	$3,142.00

Description

• Catalog Number: AB75955
• Chemical Name: Methyl 5-bromo-2-(trifluoromethyl)pyridine-4-carboxylate
• CAS Number: 1211589-41-1
• Molecular Formula: C8H5BrF3NO2
• Molecular Weight: 284.03
• MDL Number: MFCD16657895
• SMILES: COC(=O)c1cc(ncc1Br)C(F)(F)F

Computed Properties

• Complexity: 247
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• XLogP3: 2.3

Upstream Synthesis Route

Methyl 5-bromo-2-(trifluoromethyl)isonicotinate is a versatile chemical compound that plays a crucial role in chemical synthesis. It is commonly utilized as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique structure, characterized by the presence of both bromine and trifluoromethyl substituents, imparts specific reactivity and functionality to enable diverse synthetic transformations.In organic synthesis, Methyl 5-bromo-2-(trifluoromethyl)isonicotinate serves as a valuable intermediate for the introduction of both bromine and trifluoromethyl groups into target molecules. These functional groups are widely recognized for their importance in medicinal chemistry, as they can significantly enhance the biological activity and metabolic stability of the final compounds. By incorporating this compound into synthetic routes, chemists can access a wide range of novel derivatives with tailored properties for various applications.Moreover, the presence of the isonicotinate moiety in Methyl 5-bromo-2-(trifluoromethyl)isonicotinate offers additional versatility in chemical transformations. The isonicotinate scaffold is known for its diverse reactivity and compatibility with a variety of functional groups, making it an ideal platform for the construction of complex molecular architectures. Through strategic manipulations of this core structure, chemists can access diverse libraries of compounds with potential therapeutic, agricultural, or materials applications.Overall, the strategic incorporation of Methyl 5-bromo-2-(trifluoromethyl)isonicotinate in chemical synthesis enables the efficient construction of multifunctional molecules with enhanced properties. Its unique combination of bromine, trifluoromethyl, and isonicotinate functionalities provides chemists with a powerful tool for designing and accessing novel compounds with tailored characteristics for various scientific and industrial endeavors.