73841-41-5

Usage

Uses

Used in Pharmaceutical Industry:
3-Iodopyridine-2-carboxylic acid methyl ester is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or diseases.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Iodopyridine-2-carboxylic acid methyl ester is employed as a precursor in the production of pesticides and other agrochemicals. Its functional groups and chemical properties contribute to the creation of effective compounds for crop protection and enhancement of agricultural yields.
Used in Organic Synthesis:
3-Iodopyridine-2-carboxylic acid methyl ester is used as a building block in organic synthesis for the development of a wide range of chemical products. Its versatility and reactivity allow for the creation of various organic compounds with potential applications in different industries, including materials science, dyes, and specialty chemicals.
Used in Research and Development:
3-Iodopyridine-2-carboxylic acid methyl ester is also used in research and development settings to explore new chemical reactions and pathways. Its unique properties make it an interesting subject for scientific investigation, potentially leading to the discovery of novel applications and advancements in the field of chemistry.

Upstream product

• 10354-53-7 N-phenylpicolinamide 
• 67-56-1 methanol 
• 73841-32-4 3-iodopyridine-2-carboxylic acid 
• 57841-90-4 3-iodo-N-phenyl-2-pyridinecarboxamide 
• 74-88-4 methyl iodide 

Downstream Products

• 878207-38-6 3-[4-chloro-3-[(1,1-dimethylethoxy)carbonyl]phenyl]-2-pyridinecarboxylic acid methyl ester 
• 920510-95-8 methyl 3-(4-formylphenyl)-2-pyridinecarboxylate 
• 920511-16-6 methyl 3-(4-formyl-3-methoxyphenyl)-2-pyridinecarboxylate 
• 38749-98-3 (3-iodo-pyridin-2-yl)-methanol 
• 1202529-15-4 (E)-5-[1-(3-aminophenyl)propylidene]-1-isopropyl-5,10-dihydro-1H-indazolo[6,5-b]pyrido[3,2-e]oxepin 

Relevant academic research and scientific papers

An intra/intermolecular suzuki sequence to benzopyridyloxepines containing geometrically pure exocyclic tetrasubstituted alkenes

(Chemical Equation Presented) A route to enable the preparation of 5-benzylidenyl-benzopyridyloxepine analogues was developed to continue our research in the field of nuclear hormone receptor modulators. The key steps are1) a syn-stereoselective diboratio

Piperazine Heteroaryl Derivatives as Gpr38 Agonists

The invention provides compounds of formula (I) or pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, R5, R6, Z, X and B are as defined in the specification. The compounds are partial or full agonists at the GPR38 receptor. Pharmaceutical compositions comprising the compounds, methods of preparing the compounds, uses of the compounds and methods involving the compounds are also provided.

PIPERAZINE HETEROARYL DERIVATES AS GPR38 AGONISTS

The invention provides compounds of formula (I) or pharmaceutically acceptable salts thereof, (I) wherein R1, R2, R3, R4, R5, R6, Z, X and B are as defined in the specification. The compounds are partial or full agonists at the GPR38 receptor. Pharmaceutical compositions comprising the compounds, methods of preparing the compounds, uses of the compounds and methods involving the compounds are also provided.

ADAMANTYL DERIVATES AS P2X7 RECEPTOR ANTAGONISTS

The invention provides compounds of formula (I) pharmaceutically acceptable salt or solvate thereof, in which R1, A1, m and A are as defined in the specification; a process for their preparation; pharmaceutical compositions containin

NOVEL BIAROMATIC COMPOUNDS, INHIBITORS OF THE P2X7-RECEPTOR

The invention provides compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein Ar1 represents a group (II), (III), (IV) or (V), and A, Ar2, n, R1, R2, R3, R4 and R

Application of organolithium compounds in organic synthesis. Part 19. Synthetic strategies based on aromatic metallation. A concise regiospecific synthesis of 3-halogenated picolinic and isonicotinic acids

The synthesis of the halogenated picolin- and isonicotinalides (3) and (4) via metallation (n-BuLi) of the anilides (1) and (2) and then the reaction of the generated bis-lithiated anilides with halogenating agents (CCl3-CCl3, CH2Br-CH2Br, I2) followed by subsequent acidic hydrolysis of (3) and (4), as a way of regiospecific transformation of picoline and isonicotine acids into their C3-halogenated derivatives, is described.